Probes for imaging huntingtin protein

ABSTRACT

Provided are imaging agents comprising a compound of Formula I, or a pharmaceutically acceptable salt thereof, and methods of their use.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No.15/507,208, filed Feb. 27, 2017, which is the U.S. National StageApplication under 35 U.S.C. § 371 of PCT Application No.PCT/US2015/047407, filed Aug. 28, 2015, which claims priority to U.S.Provisional Application No. 62/043,603, filed Aug. 29, 2014, each ofwhich is incorporated herein by reference for all purposes.

The advent of molecular imaging approaches such as positron emissiontomography (PET) and single photon emission computed tomography (SPECT)has enabled measurements of molecular and cellular mechanisms throughoutthe body in preclinical and clinical settings. Such measurements havewidespread diagnostic utility and their use for evaluation of treatmentresponses and to assist drug development is expanding rapidly. Therecent introduction of high-resolution molecular imaging technology isconsidered by many experts as a major breakthrough that will potentiallylead to a revolutionary paradigm shift in health care and revolutionizeclinical practice.

PET involves the administration to a subject of a positron-emittingradionuclide tracer followed by detection of the positron emission(annihilation) events in the body. The radionuclide tracer is typicallycomposed of a targeting molecule having incorporated therein one or moretypes of positron-emitting radionuclides.

Many new molecular probes labeled with positron-emitting radionuclidesand associated PET imaging assays are under development to target,detect, visualize, and quantify various extracellular and intracellularmolecules and processes associated with diseases such as cancer, heartdisease, and neurological disorders. For instance, several types ofagents have been synthesized and evaluated for imaging amyloid β (Aβ)plaques in patients with Alzheimer's disease (AD) including,arylbenzothiazoles, stilbenes, imidazopyridines, pyridylbenzothiazoles,pyridylbenzoxazoles and pyridylbenzofurans (Swahn et al., Bioorganic &Medicinal Chemistry Letters, 20 (2010) 1976-1980). Furthermore,styrylbenzimidazole (SBIM) derivatives have been developed as agents forimaging neurofibrillary tangles (NFT), composed of hyperphosphorylatedtau protein, in patients with AD. In binding experiments usingrecombinant tau and amyloid β₁₋₄₂ (Aβ₁₋₄₂) aggregates,4-[(E)-2-(6-iodo-1H-benzimidazol-2-yl)ethenyl]-N,N-dimethylaniline(SBIM-3) showed higher affinity for the tau aggregates than Aβ₁₋₄₂aggregates (ratio of K_(d) values was 2.73). In in vitro autoradiographyand fluorescent staining, [¹²⁵I]SBIM-3 (or SBIM-3) bound NFT in sectionsof AD brain tissue. In biodistribution experiments using normal mice,all [¹²⁵I]SBIM derivatives showed high initial uptake into (3.20-4.11%ID/g at 2 min after the injection) and rapid clearance from (0.12-0.33%ID/g at 60 min after the injection) the brain (Matsumura et al.,Bioorganic & Medicinal Chemistry, 21 (2013) 3356-3362).

Huntington's disease (HD) is an inherited progressive neurodegenerativedisorder, characterized by motor, cognitive, and psychiatric deficits aswell as neurodegeneration and brain atrophy beginning in the striatumand the cortex and extending to other subcortical brain regions. Itbelongs to a family of neurodegenerative diseases caused by mutations inwhich an expanded CAG repeat tract results in long stretches ofpolyglutamine (polyQ) in the encoded protein. This family also includesdentatorubral-pallidoluysian atrophy (DRPLA), spinal and bulbar muscularatrophy (SBMA) and the spinocerebellar ataxias (SCAs). Apart from theirpolyQ repeats, the proteins involved are unrelated, and although theyare all widely expressed in the central nervous system and peripheraltissues, they lead to characteristic patterns of neurodegeneration. InHD, the selective neurodegeneration of the γ-aminobutyric acid-releasingspiny-projection neurons of the striatum is predominant, although lossof neurons in many other brain regions has also been reported. In theunaffected population, the number of CAG repeats in the IT₁₅ gene thatencodes the HD protein huntingtin (HTT protein) varies from 6 to 35;repeats of 36 or more define an HD allele. The length of the CAGexpansion is inversely correlated with age of disease onset, with casesof juvenile onset characterized by expansions of more than 60 repeats.HD has a prevalence of 5-10 cases per 100,000 worldwide, which makes itthe most common inherited neurodegenerative disorder. HTT protein is a348-kDa multidomain protein that contains a polymorphicglutamine/proline-rich domain at its amino-terminus. The longer polyQdomain seems to induce conformational changes in the protein, whichcauses it to form intracellular aggregates that, in most cases, manifestas nuclear inclusions. However, aggregates can also form outside thenucleus. HTT protein is present in the nucleus, cell body, dendrites andnerve terminals of neurons, and is also associated with a number oforganelles including the Golgi apparatus, endoplasmic reticulum andmitochondria.

Several clinical trials are investigating means to alleviate or reducesymptoms and slow progression in clinically diagnosed HD. Consistentwith other medical conditions, treatments might be ideally initiated ator before the earliest signs of disease. There are at least two primarychallenges to the design of clinical trials for pre-HD: selection ofparticipants who are most likely to show measurable change over thecourse of a clinical trial, and development of outcome measures that aresensitive to interventions and can demonstrate variation over thenatural history of pre-HD. In order to meet these and other challengesto preventive clinical trials, indicators of very early disease arerequired.

In view of the central role of the accumulation of aggregated forms ofHTT protein in the pathogenesis of HD, there is a need for molecularprobes that bind to such abnormalities with high sensitivity andspecificity, for molecular imaging in the living subject using PET. Thecompounds described herein meet this and other needs.

Provided is an imaging agent comprising a compound of Formula I, or apharmaceutically acceptable salt thereof,

-   -   wherein    -   X is chosen from NR₄, O and S;    -   Y is chosen from CR₄ and N;    -   Z₁, Z₂, Z₃, and Z₄ are independently chosen from CH and N,        provided that at least two of Z₁, Z₂, Z₃, and Z₄ are CH;    -   R₁ is chosen from heteroaryl, heterocycloalkenyl, and        heterocycloalkyl, each of which is optionally substituted with        one or two groups independently chosen from cyano, halo, lower        alkyl optionally substituted with amino, alkylamino, or        di(alkyl)amino, lower alkoxy optionally substituted with lower        alkoxy, optionally substituted amino, haloalkyl,        di(alkyl)aminocarbonyl, alkylaminocarbonyl, and aminocarbonyl,        or    -   R₁ is phenyl optionally substituted with one or two groups        independently chosen from cyano, heteroaryl, halo, phenoxy,        benzyloxy, heteroaryl, lower alkyl optionally substituted with        amino, (alkyl)amino, or di(alkyl)amino, lower alkoxy, optionally        substituted amino, di(alkyl)aminocarbonyl, alkylaminocarbonyl,        and aminocarbonyl;    -   L₁ is —O— and L₂ is —(CR₇R₈)_(m)— or —(CR₇R₈)_(m)—O—; or    -   L₁ is —NR₃— and L₂ is —C(O)— or —(R₇R₈)_(m)—; or    -   L₁ is —NR₃— and L₂ is —C(O)(O)(R₇R₈)_(m)—; or    -   L₁ is —NR₃— and L₂ is —C(O)(R₇R₈)_(m)(O)—; or    -   L₁ is —NR₃— and L₂ is —C(O)(R₇R₈)_(m)—; or    -   L₁ is —NR₃— and L₂ is —C(O)CR₇═CR₈—; or    -   L₁ is —C(O)— and L₂ is —NR₃; or    -   L₁ is —(R₇R₈)_(m)— and L₂ is —NR₃—, —C(O)— or —O—; or    -   L₁ is absent and L₂ is absent; or    -   L₁ taken together with L₂ is —CH═CH—, —C≡C—, or heterocyclylene;    -   L₃ is —CH═CH—, or L₃ is absent;    -   R₂ is chosen from heterocycloalkyl, aryl and heteroaryl, each of        which is optionally substituted with one or two groups chosen        from        -   —OC(O)—R₆,        -   —C(O)O—R₆,        -   amino,        -   halo,        -   haloalkyl,        -   phenyl,        -   heteroaryl,        -   cyano,        -   (lower alkyl)thio,        -   phenoxy,        -   phenoxymethyl,        -   heteroaryloxy,        -   heteroaryloxy substituted with lower alkyl,        -   hydroxyl,        -   lower alkenyloxy,        -   lower alkoxy,        -   lower alkoxy substituted with lower alkoxy, amino,            (alkyl)amino, (dialkyl)amino,        -   heterocycloalkyl, heteroaryl, or halo,        -   lower alkyl, and        -   lower alkyl substituted with amino, (alkyl)amino,            (dialkyl)amino, hydroxyl or lower alkoxy;    -   R₃ is chosen from hydrogen and lower alkyl;    -   R₄ is chosen from hydrogen, halo, cyano, and lower alkyl;    -   R₅ is chosen from lower alkyl, lower alkoxy, and halo;    -   R₆ is lower alkyl;    -   R₇ is chosen from hydrogen, hydroxyl, trifluoromethyl, and lower        alkyl;    -   R₈ is chosen from hydrogen and lower alkyl;    -   n is 0 or 1; and    -   m is 0, 1, or 2;    -   wherein the compound of Formula I, or a pharmaceutically        acceptable salt thereof, is labeled with one or more        positron-emitting radionuclides.

Also provided is a method of generating diagnostic images in anindividual comprising administering an effective amount of an imagingagent described herein to an individual, and generating an image of atleast a part of said individual.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows AUC values for the binding of ¹¹C-labeled Compound 3 ofMethod 14 in four regions of the brain in mice which are wild type, orheterozygous or homozygous for the zQ175 knock-in allele.

As used in the present specification, the following words, phrases andsymbols are generally intended to have the meanings as set forth below,except to the extent that the context in which they are used indicatesotherwise. The following abbreviations and terms have the indicatedmeanings throughout:

A dash (“-”) that is not between two letters or symbols is used toindicate a point of attachment for a substituent. For example, —CONH₂ isattached through the carbon atom.

As used herein the terms “group”, “radical” or “fragment” refer to afunctional group or fragment of a molecule attachable to a bond or otherfragments of molecules.

When a range of values is given (e.g., C₁₋₆ alkyl), each value withinthe range as well as all intervening ranges are included. For example,“C₁₋₆ alkyl” includes C₁, C₂, C₃, C₄, C₅, C₆, C₁₋₆, C₂₋₆, C₃₋₆, C₄₋₆,C₅₋₆, C₁₋₅, C₂₋₅, C₃₋₅, C₄₋₅, C₁₋₄, C₂₋₄, C₃₋₄, C₁₋₃, C₂₋₃, and C₁₋₂alkyl.

When a moiety is defined as being optionally substituted, it may besubstituted as itself or as part of another moiety. For example, ifR^(x) is defined as “C₁₋₆ alkyl or OC₁₋₆ alkyl, wherein C₁₋₆ alkyl isoptionally substituted with halogen”, then both the C₁₋₆ alkyl groupalone and the C₁₋₆ alkyl that makes up part of the OC₁₋₆ alkyl group maybe substituted with halogen.

The term “alkyl” encompasses straight chain and branched chain havingthe indicated number of carbon atoms, usually from 1 to 20 carbon atoms,for example 1 to 8 carbon atoms, such as 1 to 6 carbon atoms. Forexample C1-C6 alkyl encompasses both straight and branched chain alkylof 1 to 6 carbon atoms. Examples of alkyl groups include methyl, ethyl,propyl, isopropyl, n-butyl, sec-butyl, tert-butyl, pentyl, 2-pentyl,isopentyl, neopentyl, hexyl, 2-hexyl, 3-hexyl, 3-methylpentyl, and thelike. When an alkyl residue having a specific number of carbons isnamed, all geometric isomers having that number of carbons are intendedto be encompassed; thus, for example, “butyl” is meant to includen-butyl, sec-butyl, isobutyl and tert-butyl; “propyl” includes n-propyland isopropyl. “Lower alkyl” refers to alkyl groups having 1 to 6carbons.

By “alkoxy” is meant an alkyl group of the indicated number of carbonatoms attached through an oxygen bridge such as, for example, methoxy,ethoxy, propoxy, isopropoxy, n-butoxy, sec-butoxy, tert-butoxy, pentoxy,2-pentyloxy, isopentoxy, neopentoxy, hexoxy, 2-hexoxy, 3-hexoxy,3-methylpentoxy, and the like. Alkoxy groups will usually have from 1 to6 carbon atoms attached through the oxygen bridge. “Lower alkoxy” refersto alkoxy groups having 1 to 6 carbons. By “cycloalkoxy” is meant acycloalkyl group that is likewise attached through an oxygen bridge.

“Alkenyl” refers to an unsaturated branched or straight-chain alkylgroup having the indicated number of carbon atoms (e.g., 2 to 8 or 2 to6 carbon atoms) and at least one carbon-carbon double bond derived bythe removal of a molecule of hydrogen from adjacent carbon atoms of thecorresponding alkyl. Alkenyl groups include, but are not limited to,ethenyl, propenyl and butenyl. “Lower alkenyl” refers to alkenyl groupshaving 2 to 6 carbons.

“Alkynyl” refers to an unsaturated branched or straight-chain alkylgroup having the indicated number of carbon atoms (e.g., 2 to 8 or 2 to6 carbon atoms) and at least one carbon-carbon triple bond derived bythe removal of two molecules of hydrogen from adjacent carbon atoms ofthe corresponding alkyl. Alkynyl groups include, but are not limited to,ethynyl, propynyl (e.g., prop-1-yn-1-yl, prop-2-yn-1-yl) and butynyl(e.g., but-1-yn-1-yl, but-1-yn-3-yl, but-3-yn-1-yl). “Lower alkynyl”refers to alkynyl groups having 2 to 6 carbons.

“Aryl” indicates an aromatic carbon ring having the indicated number ofcarbon atoms, for example, 6 to 12 or 6 to 10 carbon atoms. Aryl groupsmay be monocyclic or polycyclic (e.g., bicyclic, tricyclic). In someinstances, both rings of a polycyclic aryl group are aromatic (e.g.,naphthyl). In other instances, polycyclic aryl groups may include anon-aromatic ring (e.g., cycloalkyl, cycloalkenyl, heterocycloalkyl,heterocycloalkenyl) fused to an aromatic ring, provided the polycyclicaryl group is bound to the parent structure via an atom in the aromaticring. Thus, a 1,2,3,4-tetrahydronaphthalen-5-yl group (wherein themoiety is bound to the parent structure via an aromatic carbon atom) isconsidered an aryl group, while 1,2,3,4-tetrahydronaphthalen-1-yl(wherein the moiety is bound to the parent structure via a non-aromaticcarbon atom) is not considered an aryl group. Similarly, a1,2,3,4-tetrahydroquinolin-8-yl group (wherein the moiety is bound tothe parent structure via an aromatic carbon atom) is considered an arylgroup, while 1,2,3,4-tetrahydroquinolin-1-yl group (wherein the moietyis bound to the parent structure via a non-aromatic nitrogen atom) isnot considered an aryl group. However, the term “aryl” does notencompass or overlap with “heteroaryl” regardless of the point ofattachment (e.g., both quinolin-5-yl and quinolin-2-yl are heteroarylgroups). In some instances, aryl is phenyl or naphthyl. In certaininstances, aryl is phenyl.

Bivalent radicals formed from substituted benzene derivatives and havingthe free valences at ring atoms are named as substituted phenyleneradicals. Bivalent radicals derived from univalent polycyclichydrocarbon radicals whose names end in “-yl” by removal of one hydrogenatom from the carbon atom with the free valence are named by adding“-idene” to the name of the corresponding univalent radical, e.g., anaphthyl group with two points of attachment is termed naphthylidene.

“Cycloalkyl” indicates a non-aromatic, fully saturated carbocyclic ringhaving the indicated number of carbon atoms, for example, 3 to 10, or 3to 8, or 3 to 6 ring carbon atoms. Cycloalkyl groups may be monocyclicor polycyclic (e.g., bicyclic, tricyclic). Examples of cycloalkyl groupsinclude cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl, as well asbridged and caged ring groups (e.g., norbornane, bicyclo[2.2.2]octane).In addition, one ring of a polycyclic cycloalkyl group may be aromatic,provided the polycyclic cycloalkyl group is bound to the parentstructure via a non-aromatic carbon. For example, a1,2,3,4-tetrahydronaphthalen-1-yl group (wherein the moiety is bound tothe parent structure via a non-aromatic carbon atom) is a cycloalkylgroup, while 1,2,3,4-tetrahydronaphthalen-5-yl (wherein the moiety isbound to the parent structure via an aromatic carbon atom) is notconsidered a cycloalkyl group.

“Cycloalkenyl” indicates a non-aromatic carbocyclic ring, containing theindicated number of carbon atoms (e.g., 3 to 10, or 3 to 8, or 3 to 6ring carbon atoms) and at least one carbon-carbon double bond derived bythe removal of one molecule of hydrogen from adjacent carbon atoms ofthe corresponding cycloalkyl. Cycloalkenyl groups may be monocyclic orpolycyclic (e.g., bicyclic, tricyclic). Examples of cycloalkenyl groupsinclude cyclopropenyl, cyclobutenyl, cyclopentenyl, cyclopentadienyl,and cyclohexenyl, as well as bridged and caged ring groups (e.g.,bicyclo[2.2.2]octene). In addition, one ring of a polycycliccycloalkenyl group may be aromatic, provided the polycyclic alkenylgroup is bound to the parent structure via a non-aromatic carbon atom.For example, inden-1-yl (wherein the moiety is bound to the parentstructure via a non-aromatic carbon atom) is considered a cycloalkenylgroup, while inden-4-yl (wherein the moiety is bound to the parentstructure via an aromatic carbon atom) is not considered a cycloalkenylgroup.

The term “halo” includes fluoro, chloro, bromo, and iodo, and the term“halogen” includes fluorine, chlorine, bromine, and iodine.

“Haloalkyl” includes straight and branched carbon chains having theindicated number of carbon atoms (e.g., 1 to 6 carbon atoms) substitutedwith at least one halogen atom. In instances wherein the haloalkyl groupcontains more than one halogen atom, the halogens may be the same (e.g.,dichloromethyl) or different (e.g., chlorofluoromethyl). Examples ofhaloalkyl groups include, but are not limited to, chloromethyl,dichloromethyl, trichloromethyl, fluoromethyl, difluoromethyl,trifluoromethyl, chlorofluoromethyl, 2-fluoroethyl, 2,2-difluoroethyl,2,2,2-trifluoroethyl, 1,2-difluoroethyl, 2-chloroethyl,2,2-dichloroethyl, 2,2,2-trichloroethyl, 1,2-dichloroethyl,pentachloroethyl, and pentafluoroethyl.

“Heteroaryl” indicates an aromatic ring containing the indicated numberof atoms (e.g., 5 to 12, or 5 to 10 membered heteroaryl) made up of oneor more heteroatoms (e.g., 1, 2, 3 or 4 heteroatoms) selected from N, Oand S and with the remaining ring atoms being carbon. Heteroaryl groupsdo not contain adjacent S and O atoms. In some embodiments, the totalnumber of S and O atoms in the heteroaryl group is not more than 2. Insome embodiments, the total number of S and O atoms in the heteroarylgroup is not more than 1. Unless otherwise indicated, heteroaryl groupsmay be bound to the parent structure by a carbon or nitrogen atom, asvalency permits. For example, “pyridyl” includes 2-pyridyl, 3-pyridyland 4-pyridyl groups, and “pyrrolyl” includes 1-pyrrolyl, 2-pyrrolyl and3-pyrrolyl groups. When nitrogen is present in a heteroaryl ring, itmay, where the nature of the adjacent atoms and groups permits, exist inan oxidized state (i.e., N⁺—O⁻). Additionally, when sulfur is present ina heteroaryl ring, it may, where the nature of the adjacent atoms andgroups permits, exist in an oxidized state (i.e., S⁺—O⁻ or SO₂).Heteroaryl groups may be monocyclic or polycyclic (e.g., bicyclic,tricyclic).

In some instances, a heteroaryl group is monocyclic. Examples includepyrrole, pyrazole, imidazole, triazole (e.g., 1,2,3-triazole,1,2,4-triazole, 1,3,4-triazole), tetrazole, furan, isoxazole, oxazole,oxadiazole (e.g., 1,2,3-oxadiazole, 1,2,4-oxadiazole, 1,3,4-oxadiazole),thiophene, isothiazole, thiazole, thiadiazole (e.g., 1,2,3-thiadiazole,1,2,4-thiadiazole, 1,3,4-thiadiazole), pyridine, pyridazine, pyrimidine,pyrazine, triazine (e.g., 1,2,4-triazine, 1,3,5-triazine) and tetrazine.

In some instances, both rings of a polycyclic heteroaryl group arearomatic. Examples include indole, isoindole, indazole, benzimidazole,benzotriazole, benzofuran, benzoxazole, benzisoxazole, benzoxadiazole,benzothiophene, benzothiazole, benzoisothiazole, benzothiadiazole,1H-pyrrolo[2,3-b]pyridine, 1H-pyrazolo[3,4-b]pyridine,3H-imidazo[4,5-b]pyridine, 3H-[1,2,3]triazolo[4,5-b]pyridine,1H-pyrrolo[3,2-b]pyridine, 1H-pyrazolo[4,3-b]pyridine,1H-imidazo[4,5-b]pyridine, 1H-[1,2,3]triazolo[4,5-b]pyridine,1H-pyrrolo[2,3-c]pyridine, 1H-pyrazolo[3,4-c]pyridine,3H-imidazo[4,5-c]pyridine, 3H-[1,2,3]triazolo[4,5-c]pyridine,1H-pyrrolo[3,2-c]pyridine, 1H-pyrazolo[4,3-c]pyridine,1H-imidazo[4,5-c]pyridine, 1H-[1,2,3]triazolo[4,5-c]pyridine,furo[2,3-b]pyridine, oxazolo[5,4-b]pyridine, isoxazolo[5,4-b]pyridine,[1,2,3]oxadiazolo[5,4-b]pyridine, furo[3,2-b]pyridine,oxazolo[4,5-b]pyridine, isoxazolo[4,5-b]pyridine,[1,2,3]oxadiazolo[4,5-b]pyridine, furo[2,3-c]pyridine,oxazolo[5,4-c]pyridine, isoxazolo[5,4-c]pyridine,[1,2,3]oxadiazolo[5,4-c]pyridine, furo[3,2-c]pyridine,oxazolo[4,5-c]pyridine, isoxazolo[4,5-c]pyridine,[1,2,3]oxadiazolo[4,5-c]pyridine, thieno[2,3-b]pyridine,thiazolo[5,4-b]pyridine, isothiazolo[5,4-b]pyridine,[1,2,3]thiadiazolo[5,4-b]pyridine, thieno[3,2-b]pyridine,thiazolo[4,5-b]pyridine, isothiazolo[4,5-b]pyridine,[1,2,3]thiadiazolo[4,5-b]pyridine, thieno[2,3-c]pyridine,thiazolo[5,4-c]pyridine, isothiazolo[5,4-c]pyridine,[1,2,3]thiadiazolo[5,4-c]pyridine, thieno[3,2-c]pyridine,thiazolo[4,5-c]pyridine, isothiazolo[4,5-c]pyridine,[1,2,3]thiadiazolo[4,5-c]pyridine, quinoline, isoquinoline, cinnoline,quinazoline, quinoxaline, phthalazine, naphthyridine (e.g.,1,8-naphthyridine, 1,7-naphthyridine, 1,6-naphthyridine,1,5-naphthyridine, 2,7-naphthyridine, 2,6-naphthyridine),imidazo[1,2-a]pyridine, 1H-pyrazolo[3,4-d]thiazole,1H-pyrazolo[4,3-d]thiazole and imidazo[2,1-b]thiazole.

In other instances, polycyclic heteroaryl groups may include anon-aromatic ring (e.g., cycloalkyl, cycloalkenyl, heterocycloalkyl,heterocycloalkenyl) fused to a heteroaryl ring, provided the polycyclicheteroaryl group is bound to the parent structure via an atom in thearomatic ring. For example, a 4,5,6,7-tetrahydrobenzo[d]thiazol-2-ylgroup (wherein the moiety is bound to the parent structure via anaromatic carbon atom) is considered a heteroaryl group, while4,5,6,7-tetrahydrobenzo[d]thiazol-5-yl (wherein the moiety is bound tothe parent structure via a non-aromatic carbon atom) is not considered aheteroaryl group.

“Heterocycloalkyl” indicates a non-aromatic, fully saturated ring havingthe indicated number of atoms (e.g., 3 to 10, or 3 to 7, memberedheterocycloalkyl) made up of one or more heteroatoms (e.g., 1, 2, 3 or 4heteroatoms) selected from N, O and S and with the remaining ring atomsbeing carbon. Heterocycloalkyl groups may be monocyclic or polycyclic(e.g., bicyclic, tricyclic).

Examples of monocyclic heterocycloalkyl groups include oxiranyl,aziridinyl, azetidinyl, pyrrolidinyl, imidazolidinyl, pyrazolidinyl,piperidinyl, piperazinyl, morpholinyl and thiomorpholinyl.

When nitrogen is present in a heterocycloalkyl ring, it may, where thenature of the adjacent atoms and groups permits, exist in an oxidizedstate (i.e., N⁺—O⁻). Examples include piperidinyl N-oxide andmorpholinyl-N-oxide. Additionally, when sulfur is present in aheterocycloalkyl ring, it may, where the nature of the adjacent atomsand groups permits, exist in an oxidized state (i.e., S⁺—O⁻ or —SO₂—).Examples include thiomorpholine S-oxide and thiomorpholine S,S-dioxide.

In addition, one ring of a polycyclic heterocycloalkyl group may bearomatic (e.g., aryl or heteroaryl), provided the polycyclicheterocycloalkyl group is bound to the parent structure via anon-aromatic carbon or nitrogen atom. For example, a1,2,3,4-tetrahydroquinolin-1-yl group (wherein the moiety is bound tothe parent structure via a non-aromatic nitrogen atom) is considered aheterocycloalkyl group, while 1,2,3,4-tetrahydroquinolin-8-yl group(wherein the moiety is bound to the parent structure via an aromaticcarbon atom) is not considered a heterocycloalkyl group.

“Heterocycloalkenyl” indicates a non-aromatic ring having the indicatednumber of atoms (e.g., 3 to 10, or 3 to 7, membered heterocycloalkyl)made up of one or more heteroatoms (e.g., 1, 2, 3 or 4 heteroatoms)selected from N, O and S and with the remaining ring atoms being carbon,and at least one double bond derived by the removal of one molecule ofhydrogen from adjacent carbon atoms, adjacent nitrogen atoms, oradjacent carbon and nitrogen atoms of the correspondingheterocycloalkyl. Heterocycloalkenyl groups may be monocyclic orpolycyclic (e.g., bicyclic, tricyclic). When nitrogen is present in aheterocycloalkenyl ring, it may, where the nature of the adjacent atomsand groups permits, exist in an oxidized state (i.e., N⁺—O⁻).Additionally, when sulfur is present in a heterocycloalkenyl ring, itmay, where the nature of the adjacent atoms and groups permits, exist inan oxidized state (i.e., S⁺—O⁻ or —SO₂—). Examples of heterocycloalkenylgroups include dihydrofuranyl (e.g., 2,3-dihydrofuranyl,2,5-dihydrofuranyl), dihydrothiophenyl (e.g., 2,3-dihydrothiophenyl,2,5-dihydrothiophenyl), dihydropyrrolyl (e.g., 2,3-dihydro-1H-pyrrolyl,2,5-dihydro-1H-pyrrolyl), dihydroimidazolyl (e.g.,2,3-dihydro-1H-imidazolyl, 4,5-dihydro-1H-imidazolyl), pyranyl,dihydropyranyl (e.g., 3,4-dihydro-2H-pyranyl, 3,6-dihydro-2H-pyranyl),tetrahydropyridinyl (e.g., 1,2,3,4-tetrahydropyridinyl,1,2,3,6-tetrahydropyridinyl) and dihydropyridine (e.g.,1,2-dihydropyridine, 1,4-dihydropyridine). In addition, one ring of apolycyclic heterocycloalkenyl group may be aromatic (e.g., aryl orheteroaryl), provided the polycyclic heterocycloalkenyl group is boundto the parent structure via a non-aromatic carbon or nitrogen atom. Forexample, a 1,2-dihydroquinolin-1-yl group (wherein the moiety is boundto the parent structure via a non-aromatic nitrogen atom) is considereda heterocycloalkenyl group, while 1,2-dihydroquinolin-8-yl group(wherein the moiety is bound to the parent structure via an aromaticcarbon atom) is not considered a heterocycloalkenyl group.

The term “heterocyclylene” as used herein refers to a non-aromaticmonocyclic di-radical having 3- to 5-ring atoms. Examples ofheterocyclylene include 1,2-oxiranylene, 2,2-oxiranylene,1,2-aziridinylene, 2,2-aziridinylene, 2,2-oxetanylene, 2,3-oxetanylene,2,4-oxetanylene, 3,3-oxetanylene, 2,2-azetindinylene,2,3-azetindinylene, 2,3-azetindinylene, 3,3-azetindinylene,2,3-tetrahydrofuranylene, and 3,4-tetrahydrofuranylene.

By “optional” or “optionally” is meant that the subsequently describedevent or circumstance may or may not occur, and that the descriptionincludes instances where the event or circumstance occurs and instancesin which it does not. For example, “optionally substituted alkyl”encompasses both “alkyl” and “substituted alkyl” as defined herein. Itwill be understood by those skilled in the art, with respect to anygroup containing one or more substituents, that such groups are notintended to introduce any substitution or substitution patterns that aresterically impractical, synthetically non-feasible, and/or inherentlyunstable.

The term “substituted”, as used herein, means that any one or morehydrogens on the designated atom or group is replaced with a selectionfrom the indicated group, provided that the designated atom's normalvalence is not exceeded. When a substituent is oxo (i.e., ═O) then 2hydrogens on the atom are replaced. Combinations of substituents and/orvariables are permissible only if such combinations result in stablecompounds or useful synthetic intermediates. A stable compound or stablestructure is meant to imply a compound that is sufficiently robust tosurvive isolation from a reaction mixture, and subsequent formulation asan agent having at least practical utility. Unless otherwise specified,substituents are named into the core structure. For example, it is to beunderstood that when (cycloalkyl)alkyl is listed as a possiblesubstituent, the point of attachment of this substituent to the corestructure is in the alkyl portion.

The terms “substituted” alkyl (including without limitation C₁-C₄alkyl), cycloalkyl, cycloalkenyl, aryl, heterocycloalkyl,heterocycloalkenyl, and heteroaryl, unless otherwise expressly defined,refer respectively to alkyl, cycloalkyl, cycloalkenyl, aryl,heterocycloalkyl, heterocycloalkenyl, and heteroaryl, herein one or more(such as up to 5, for example, up to 3) hydrogen atoms are replaced by asubstituent independently chosen from: —R^(a), —OR^(b), —O(C₁-C₂alkyl)O— (e.g., methylenedioxy-), —SR^(b), guanidine (—NHC(═NH)NH₂),guanidine wherein one or more of the guanidine hydrogens are replacedwith a C₁-C₄alkyl group, —NR^(b)R^(c), halo, cyano, oxo (as asubstituent for heterocycloalkyl), nitro, —COR^(b), —CO₂R^(b),—CONR^(b)R^(c), —OCOR^(b), —OCO₂R^(a), —OCONR^(b)R^(c), —NR^(c)COR^(b),—NR^(c)CO₂R^(a), —NR^(c)CONR^(b)R^(c), —SOR^(a), —SO₂R^(a),—SO₂NR^(b)R^(c), and —NR^(c)SO₂R^(a),

where R^(a) is chosen from C₁-C₆ alkyl, cycloalkyl, aryl,heterocycloalkyl, and heteroaryl;

R^(b) is chosen from H, C₁-C₆ alkyl, aryl, and heteroaryl; and

R^(c) is chosen from hydrogen and C₁-C₆ alkyl; or

R^(b) and R^(c), and the nitrogen to which they are attached, form aheterocycloalkyl group; and where each C₁-C₆ alkyl, cycloalkyl, aryl,heterocycloalkyl, and heteroaryl is optionally substituted with one ormore, such as one, two, or three, substituents independently selectedfrom C₁-C₄ alkyl, C₃-C₆ cycloalkyl, aryl, heteroaryl, aryl-C₁-C₄ alkyl-,heteroaryl-C₁-C₄ alkyl-, C₁-C₄ haloalkyl-, —OC₁-C₄ alkyl, —OC₁-C₄alkylphenyl, —C₁-C₄ alkyl-OH, —C₁-C₄ alkyl-O—C₁-C₄ alkyl, —OC₁-C₄haloalkyl, halo, —OH, —NH₂, —C₁-C₄ alkyl-NH₂, —N(C₁-C₄ alkyl)(C₁-C₄alkyl), —N(C₁-C₄ alkyl)(C₁-C₄ alkylheteroaryl), —NH(C₁-C₄ alkyl),—N(C₁-C₄ alkyl)(C₁-C₄ alkylphenyl), —NH(C₁-C₄ alkylphenyl), cyano,nitro, oxo (as a substitutent for heteroaryl), —CO₂H, —C(O)OC₁-C₄ alkyl,—CON(C₁-C₄ alkyl)(C₁-C₄ alkyl), —CONH(C₁-C₄ alkyl), —CONH₂,—NHC(O)(C₁-C₄ alkyl), —NHC(O)(phenyl), —N(C₁-C₄ alkyl)C(O)(C₁-C₄ alkyl),—N(C₁-C₄ alkyl)C(O)(phenyl), —C(O)C₁-C₄ alkyl, —C(O)C₁-C₄ phenyl,—C(O)C₁-C₄ haloalkyl, —OC(O)C₁-C₄ alkyl, —SO₂(C₁-C₄ alkyl),—SO₂(phenyl), —SO₂(C₁-C₄ haloalkyl), —SO₂NH₂, —SO₂NH(C₁-C₄ alkyl),—SO₂NH(phenyl), —NHSO₂(C₁-C₄ alkyl), —NHSO₂(phenyl), and —NHSO₂(C₁-C₄haloalkyl).

The term “substituted amino” refers to the group —NHR^(d) or—NR^(d)R^(d) where each R^(d) is independently chosen from: optionallysubstituted alkyl, optionally substituted cycloalkyl, optionallysubstituted acyl, optionally substituted aryl, optionally substitutedheteroaryl, optionally substituted heterocycloalkyl, alkoxycarbonyl,sulfinyl and sulfonyl, wherein substituted alkyl, cycloalkyl, aryl,heterocycloalkyl, and heteroaryl refer respectively to alkyl,cycloalkyl, aryl, heterocycloalkyl, and heteroaryl wherein one or more(such as up to 5, for example, up to 3) hydrogen atoms are replaced by asubstituent independently chosen from:

—R^(a), —OR^(b), —O(C₁-C₂ alkyl)O— (e.g., methylenedioxy-), —SR^(b),guanidine, guanidine wherein one or more of the guanidine hydrogens arereplaced with a lower-alkyl group, —NR^(b)R^(c), halo, cyano, nitro,—COR^(b), —CO₂R^(b), —CONR^(b)R^(c), —OCOR^(b), —OCO₂R^(a),—OCONR^(b)R^(c), —NR^(c)COR^(b), —NR^(c)CO₂R^(a), —NR^(c)CONR^(b)R^(c),—CO₂R^(b), —CONR^(b)R^(c), —NR^(c)COR^(b), —SOR^(a), —SO₂R^(a),—SO₂NR^(b)R^(c), and —NR^(c)SO₂R^(a),

where R^(a) is chosen from optionally substituted C₁-C₆ alkyl,optionally substituted aryl, and optionally substituted heteroaryl;

R^(b) is chosen from H, optionally substituted C₁-C₆ alkyl, optionallysubstituted aryl, and optionally substituted heteroaryl; and

R^(c) is chosen from hydrogen and optionally substituted C₁-C₄ alkyl;

where each optionally substituted group is unsubstituted orindependently substituted with one or more, such as one, two, or three,substituents independently selected from C₁-C₄ alkyl, aryl, heteroaryl,aryl-C₁-C₄ alkyl-, heteroaryl-C₁-C₄ alkyl-, C₁-C₄ haloalkyl-, —OC₁-C₄alkyl, —OC₁-C₄ alkylphenyl, —C₁-C₄ alkyl-OH, —OC₁-C₄ haloalkyl, halo,—OH, —NH₂, —C₁-C₄ alkyl-NH₂, —N(C₁-C₄ alkyl)(C₁-C₄ alkyl), —NH(C₁-C₄alkyl), —N(C₁-C₄ alkyl)(C₁-C₄ alkylphenyl), —N(C₁-C₄ alkyl)(C₁-C₄alkylheteroaryl), —NH(C₁-C₄ alkylphenyl), cyano, nitro, oxo (as asubstitutent for heteroaryl), —CO₂H, —C(O)OC₁-C₄ alkyl, —CON(C₁-C₄alkyl)(C₁-C₄ alkyl), —CONH(C₁-C₄ alkyl), —CONH₂, —NHC(O)(C₁-C₄ alkyl),—NHC(O)(phenyl), —N(C₁-C₄ alkyl)C(O)(C₁-C₄ alkyl), —N(C₁-C₄alkyl)C(O)(phenyl), —C(O)C₁-C₄ alkyl, —C(O)C₁-C₄ phenyl, —C(O)C₁-C₄haloalkyl, —OC(O)C₁-C₄ alkyl, —SO₂(C₁-C₄ alkyl), —SO₂(phenyl),—SO₂(C₁-C₄ haloalkyl), —SO₂NH₂, —SO₂NH(C₁-C₄ alkyl), —SO₂NH(phenyl),—NHSO₂(C₁-C₄ alkyl), —NHSO₂(phenyl), and —NHSO₂(C₁-C₄ haloalkyl).

The term “substituted amino” also refers to the group —NR^(e)R^(f)wherein R^(e) and R^(f), together with the nitrogen to which they arebound, form an optionally substituted 5- to 7-memberednitrogen-containing, non-aromatic, heterocycle which optionally contains1 or 2 additional heteroatoms chosen from nitrogen, oxygen, and sulfur.

“Aminocarbonyl” encompasses a group of the formula —(C═O)(optionallysubstituted amino) wherein substituted amino is as described herein.

Compounds described herein include, but are not limited to, theiroptical isomers, racemates, and other mixtures thereof. In thosesituations, the single enantiomers or diastereoisomers, i.e., opticallyactive forms, can be obtained by asymmetric synthesis or by resolutionof the racemates. Resolution of the racemates can be accomplished, forexample, by conventional methods such as crystallization in the presenceof a resolving agent, or chromatography, using, for example a chiralhigh-pressure liquid chromatography (HPLC) column. The term “isomers”refers to different compounds that have the same molecular formula. Theterm “stereoisomers” refers to isomers that differ only in the way theatoms are arranged in space. The term “enantiomers” refers tostereoisomers that are non-superimposable mirror images of each other. A1:1 mixture of a pair of enantiomers is a “racemic” mixture. The symbol“(±)” may be used to designate a racemic mixture where appropriate. Theterm “diastereoisomers” refers to stereoisomers that have at least twoasymmetric atoms, but which are not mirror-images of each other. Theabsolute stereochemistry is specified according to theCahn-Ingold-Prelog R-S system. When a compound is a pure enantiomer thestereochemistry at each chiral carbon can be specified by either R or S.Resolved compounds whose absolute configuration is unknown can bedesignated (+) or (−) depending on the direction (dextro- orlevorotatory) which they rotate plane polarized light at the wavelengthof the sodium D line. The absolute stereochemistry of substituted doublebonds may be designated E or Z according to the priority rules of theCahn-Ingold-Prelog system.

Where compounds described herein exist in various tautomeric forms, theterm “compound” includes all tautomeric forms of the compound. Suchcompounds also include crystal forms including polymorphs andclathrates. Similarly, the term “salt” includes all tautomeric forms andcrystal forms of the compound. The term “tautomers” refers tostructurally distinct isomers that interconvert by tautomerization.Tautomerization is a form of isomerization and includes prototropic orproton-shift tautomerization, which is considered a subset of acid-basechemistry. Prototropic tautomerization or proton-shift tautomerizationinvolves the migration of a proton accompanied by changes in bond order,often the interchange of a single bond with an adjacent double bond.Where tautomerization is possible (e.g. in solution), a chemicalequilibrium of tautomers can be reached. An example of tautomerizationis keto-enol tautomerization. A specific example of keto-enoltautomerization is the interconversion of pentane-2,4-dione and4-hydroxypent-3-en-2-one tautomers. Another example of tautomerizationis phenol-keto tautomerization. A specific example of phenol-ketotautomerization is the interconversion of pyridin-4-ol andpyridin-4(1H)-one tautomers.

Pharmaceutically acceptable forms of the compounds recited hereininclude pharmaceutically acceptable salts, and mixtures thereof. In someembodiments, the compounds described herein are in the form ofpharmaceutically acceptable salts.

“Pharmaceutically acceptable salts” include, but are not limited tosalts with inorganic acids, such as hydrochlorate, phosphate,diphosphate, hydrobromate, sulfate, sulfinate, nitrate, and like salts;as well as salts with an organic acid, such as malate, maleate,fumarate, tartrate, succinate, citrate, lactate, methanesulfonate,p-toluenesulfonate, 2-hydroxyethylsulfonate, benzoate, salicylate,stearate, haloalkanoate such as trifluoroacetate, and alkanoate such asacetate, HOOC—(CH₂)_(n)—COOH where n is 0-4, and like salts. Similarly,pharmaceutically acceptable cations include, but are not limited tosodium, potassium, calcium, aluminum, lithium, and ammonium. Inaddition, if the compounds described herein are obtained as an acidaddition salt, the free base can be obtained by basifying a solution ofthe acid salt. Conversely, if the product is a free base, an additionsalt, particularly a pharmaceutically acceptable addition salt, may beproduced by dissolving the free base in a suitable organic solvent andtreating the solution with an acid, in accordance with conventionalprocedures for preparing acid addition salts from base compounds. Thoseskilled in the art will recognize various synthetic methodologies thatmay be used to prepare non-toxic pharmaceutically acceptable additionsalts.

The term “administering”, as used herein in conjunction with adiagnostic agent, such as, for example, a positron-emitter labeledcompound described herein, means administering directly into or onto atarget tissue or to administer the diagnostic agent systemically to apatient whereby the diagnostic agent is used to image the tissue or apathology associated with the tissue to which it is targeted.“Administering” a composition may be accomplished by injection,infusion, or by either method in combination with other knowntechniques.

The term “Curie” (Ci) is a unit of measurement of radioactivity. One Cirefers to that amount of any radioactive material that will decay at arate of 3.7×10¹⁰ disintegrations per second. The term “milliCurie” (mCi)refers to 10⁻³ Curie. It is understood that the International System(SI) unit of radioactivity, the Becquerel, is equal to onedisintegration/second. Thus one Becquerel=2.7×10⁻¹¹ Curie.

The term “diagnostic imaging”, as used herein, refers to the use ofelectromagnetic radiation to produce images of internal structures ofthe human or animal body for the purpose of diagnosis.

The term “effective amount” of a compound, as used herein, is apredetermined amount calculated to achieve a desired effect such as anamount sufficient to enable the acquisition of a desired image of thetarget organ of an individual. In some instances the target organ is thebrain.

The term “huntingtin protein” or “HTT protein”, as used herein, refersto the protein encoded by the human huntingtin gene (HTT gene) locatedon the short (p) arm of chromosome 4 at position 16.3. More precisely,the IT₁₅ gene coding for the HTT protein is located from base pair3,076,407 to base pair 3,245,686 on chromosome 4.

The term “HTT protein aggregate”, as used herein refers to an insolublefibrous amyloid comprising mis-folded HTT protein molecules.

The term “β-amyloid aggregate”, as used herein refers to an insolublefibrous amyloid comprising mis-folded β-amyloid protein molecules.

The term “imaging agent”, as used herein, refers to a compound asdescribed herein labeled with one or more positron-emitting isotopes orradionuclides. A positron-emitter labeled compound need only be enrichedwith a detectable isotope to a degree that permits detection with atechnique suitable for the particular application.

The term “pathologic process”, as used herein, refers to an alteredendogenous biological process that may be associated with the aberrantproduction and/or functioning of proteins, peptides, RNA and othersubstances associated with such biological process.

The term “PET imaging”, as used herein, refers to the use of apositron-emitter labeled compound to produce images of internalstructures of the human or animal body.

The term “pharmaceutical composition” refers to a composition comprisingat least one imaging agent described herein, whereby the composition isamenable to investigation for a specified, efficacious outcome in amammal (for example, without limitation, a human). Those of ordinaryskill in the art will understand and appreciate the techniquesappropriate for determining whether a composition has a desiredefficacious outcome based upon the needs of the artisan.

The term “positron-emitting radionuclide”, as used herein, refers to aradio-active isotope that exhibits particular type of radioactive decayreferred to as β+ decay, in which a proton inside a radionuclide nucleusis converted into a neutron while releasing a positron and an electronneutrino (ν_(e)). Some examples of positron-emitting radionuclidesinclude ¹⁵O, ¹³N, ¹¹C, ¹⁸F, ⁷⁶Br, and ¹²⁴I. These radionuclides havehalf-lives of about 2, 10, 20, 110 minutes, 16 hours, and 4.2 daysrespectively.

The term “tomography”, as used herein, refers to a process of imaging bysections. The images may be looked at individually, as a series oftwo-dimensional slices or together, as a computer-generatedthree-dimensional representation.

Provided is an imaging agent comprising a compound of Formula I, or apharmaceutically acceptable salt thereof,

-   -   wherein    -   X is chosen from NR₄, O and S;    -   Y is chosen from CR₄ and N;    -   Z₁, Z₂, Z₃, and Z₄ are independently chosen from CH and N,        provided that at least two of Z₁, Z₂, Z₃, and Z₄ are CH;    -   R₁ is chosen from heteroaryl, heterocycloalkenyl, and        heterocycloalkyl, each of which is optionally substituted with        one or two groups independently chosen from cyano, halo, lower        alkyl optionally substituted with amino, alkylamino, or        di(alkyl)amino, lower alkoxy optionally substituted with lower        alkoxy, optionally substituted amino, haloalkyl,        di(alkyl)aminocarbonyl, alkylaminocarbonyl, and aminocarbonyl,        or    -   R₁ is phenyl optionally substituted with one or two groups        independently chosen from cyano, heteroaryl, halo, phenoxy,        benzyloxy, heteroaryl, lower alkyl optionally substituted with        amino, (alkyl)amino, or di(alkyl)amino, lower alkoxy, optionally        substituted amino, di(alkyl)aminocarbonyl, alkylaminocarbonyl,        and aminocarbonyl;    -   L₁ is —O— and L₂ is —(CR₇R₈)_(m)— or —(CR₇R₈)_(m)—O—; or    -   L₁ is —NR₃— and L₂ is —C(O)— or —(R₇R₈)_(m)—; or    -   L₁ is —NR₃— and L₂ is —C(O)(O)(R₇R₈)_(m)—; or    -   L₁ is —NR₃— and L₂ is —C(O)(R₇R₈)_(m)(O)—; or    -   L₁ is —NR₃— and L₂ is —C(O)(R₇R₈)_(m)—; or    -   L₁ is —NR₃— and L₂ is —C(O)CR₇═CR₈—; or    -   L₁ is —C(O)— and L₂ is —NR₃; or    -   L₁ is —(R₇R₈)_(m)— and L₂ is —NR₃—, —C(O)— or —O—; or    -   L₁ is absent and L₂ is absent; or    -   L₁ taken together with L₂ is —CH═CH—, —C≡C—, or heterocyclylene;    -   L₃ is —CH═CH—, or L₃ is absent;    -   R₂ is chosen from heterocycloalkyl, aryl and heteroaryl, each of        which is optionally substituted with one or two groups chosen        from        -   —OC(O)—R₆,        -   —C(O)O—R₆,        -   amino,        -   halo,        -   haloalkyl,        -   phenyl,        -   heteroaryl,        -   cyano,        -   (lower alkyl)thio,        -   phenoxy,        -   phenoxymethyl,        -   heteroaryloxy,        -   heteroaryloxy substituted with lower alkyl,        -   hydroxyl,        -   lower alkenyloxy,        -   lower alkoxy,        -   lower alkoxy substituted with lower alkoxy, amino,            (alkyl)amino, (dialkyl)amino, heterocycloalkyl, heteroaryl,            or halo,        -   lower alkyl, and        -   lower alkyl substituted with amino, (alkyl)amino,            (dialkyl)amino, hydroxyl or lower alkoxy;    -   R₃ is chosen from hydrogen and lower alkyl;    -   R₄ is chosen from hydrogen, halo, cyano, and lower alkyl;    -   R₅ is chosen from lower alkyl, lower alkoxy, and halo;    -   R₆ is lower alkyl;    -   R₇ is chosen from hydrogen, hydroxyl, trifluoromethyl, and lower        alkyl;    -   R₈ is chosen from hydrogen and lower alkyl;    -   n is 0 or 1; and    -   m is 0, 1, or 2;    -   wherein the compound of Formula I, or a pharmaceutically        acceptable salt thereof, is labeled with one or more        positron-emitting radionuclides.

Provided is an imaging agent comprising a compound of Formula I, or apharmaceutically acceptable salt thereof,

-   -   wherein    -   X is chosen from NR₄, O and S;    -   Y is chosen from CR₄ and N;    -   Z₁, Z₂, Z₃, and Z₄ are independently chosen from CH and N,        provided that at least two of Z₁, Z₂, Z₃, and Z₄ are CH;    -   R₁ is chosen from heteroaryl and heterocycloalkyl, each of which        is optionally substituted with one or two groups independently        chosen from cyano, halo, lower alkyl, lower alkoxy optionally        substituted with lower alkoxy, optionally substituted amino, and        aminocarbonyl, or    -   R₁ is phenyl optionally substituted with one or two groups        independently chosen from cyano, halo, lower alkyl optionally        substituted with amino, (alkyl)amino, or di(alkyl)amino, lower        alkoxy, optionally substituted amino, and aminocarbonyl;    -   L₁ is —O— and L₂ is —(CR₇R₈)_(m)— or —(CR₇R₈)_(m)—O—; or    -   L₁ is —NR₃— and L₂ is —C(O)— or —(R₇R₈)_(m)—; or    -   L₁ is —(R₇R₈)_(m)— and L₂ is —NR₃—, —C(O)— or —O—; or    -   L₁ is absent and L₂ is absent; or    -   L₁ taken together with L₂ is —CH═CH—, —C≡C—, or heterocyclylene;    -   R₂ is chosen from heterocycloalkyl, aryl and heteroaryl, each of        which is optionally substituted with one or two groups chosen        from        -   —OC(O)—R₆,        -   hydroxyl,        -   lower alkenyloxy,        -   lower alkoxy,        -   lower alkoxy substituted with lower alkoxy, amino,            (alkyl)amino, (dialkyl)amino, heterocycloalkyl, or halo,        -   lower alkyl, and        -   lower alkyl substituted with amino, (alkyl)amino,            (dialkyl)amino, hydroxyl or lower alkoxy;    -   R₃ is chosen from hydrogen and lower alkyl;    -   R₄ is chosen from hydrogen, halo, cyano, and lower alkyl;    -   R₅ is chosen from lower alkyl, lower alkoxy, and halo;    -   R₆ is lower alkyl;    -   R₇ is chosen from hydrogen, hydroxyl, trifluoromethyl, and lower        alkyl;    -   R₈ is chosen from hydrogen and lower alkyl;    -   n is 0 or 1; and    -   m is 0, 1, or 2;    -   wherein the compound of Formula I, or a pharmaceutically        acceptable salt thereof, is labeled with one or more        positron-emitting radionuclides.

In some embodiments, X is O.

In some embodiments, X is S.

In some embodiments, X is NR₄.

In some embodiments, Y is CR₄.

In some embodiments, R₄ is hydrogen. In some embodiments, R₄ is halo. Insome embodiments, R₄ is bromo. In some embodiments, R₄ is cyano. In someembodiments, R₄ is lower alkyl. In some embodiments, R₄ is methyl.

In some embodiments, Y is N.

In some embodiments, Z₁, Z₂, Z₃, and Z₄ are CH.

In some embodiments, Z₁ is N and Z₂, Z₃, and Z₄ are CH.

In some embodiments, Z₂ is N and Z₁, Z₃, and Z₄ are CH.

In some embodiments, Z₂ and Z₄ are N and Z₁ and Z₃ are CH.

In some embodiments, R₁ is chosen from phenyl, pyridine-2-yl,pyridine-3-yl, pyridine-3-yl-1-oxide, pyridine-4-yl, 1H-pyrazol-4-yl,pyrazin-2-yl, pyridazin-3-yl, pyridazin-4-yl, pyrimidin-4-yl,pyrimidin-5-yl, 2,3-dihydropyridazin-3-one-6-yl,1,2-dihydropyridin-2-one-5-yl, 1,2-dihydropyrazin-2-one-5-yl,1,3-thiazol-5-yl, 5,6,7,8-tetrahydro-1,7-naphthyridine-7-yl,1H-imidazol-1-yl, 1-benzofuran-2-yl, 1-benzofuran-5-yl,2,3-dihydro-1-benzofuran-2-yl, quinolone-2-yl, and5H,6H,7H,8H-imidazo[1,2-a]pyrazin-7-yl, each of which is optionallysubstituted with one or two groups independently chosen from halo, loweralkyl, lower alkoxy, and optionally substituted amino.

In some embodiments R₁ is

-   -   wherein    -   W is chosen from CH, N, and N(O);    -   p is chosen from 0, 1, and 2;    -   for each occurrence, R₉ is independently chosen from cyano,        halo, lower alkyl, lower haloalkyl, lower alkyl substituted with        —NR₁₀R₁₁, lower alkoxy, —C(O)NR₁₀R₁₁, and —NR₁₀R₁₁;    -   R₁₀ is chosen from hydrogen and lower alkyl;    -   R₁₁ is chosen from hydrogen, lower alkyl, and —C(O)R₁₂; and    -   R₁₂ is chosen from hydrogen and lower alkyl.

In some embodiments,

-   -   W is chosen from CH and N;    -   p is chosen from 0, 1, and 2;    -   for each occurrence, R₉ is independently chosen from cyano,        halo, lower alkyl, lower alkoxy, —C(O)NR₁₀R₁₁, and —NR₁₀R₁₁    -   R₁₀ is chosen from hydrogen and lower alkyl;    -   R₁₁ is chosen from hydrogen, lower alkyl, and —C(O)R₁₂; and    -   R₁₂ is chosen from hydrogen and lower alkyl.

In some embodiments, W is CH. In some embodiments, W is N. In someembodiments, W is N(O).

In some embodiments, p is 0.

In some embodiments, p is 1.

In some embodiments, R₉ is chosen from cyano, halo, methyl, and methoxy.

In some embodiments, R₁ is

-   -   wherein    -   W₁ and W₂ are chosen from CH and N, provided that at least one        of W₁ and W₂ is CH;    -   p is chosen from 0, 1, and 2; and    -   for each occurrence, R₉ is independently chosen from lower        alkyl. In some embodiments, R₁ is 1H-pyrazol-4-yl optionally        substituted with lower alkyl.

In some embodiments, L₁ is —O— and L₂ is —(CR₇R₈)_(m)- or—(CR₇R₈)_(m)—O—. In some embodiments, L₁ is —O— and L₂ is —(CR₇R₈)_(m)—.

In some embodiments, L₁ is —O—, L₂ is —(CR₇R₈)_(m)- or —(CR₇R₈)_(m)—O—and R₂ is phenyl, pyridine-2-yl, pyridine-3-yl, pyrazin-2-yl,pyrimidine-5-yl, 1H-imidazol-4-yl, 1H-imidazol-2-yl, or 1H-pyrazol-4-yl,each of which is optionally substituted with one or two groupsindependent chosen from lower alkyl, hydroxyl, lower alkoxy, loweralkoxy substituted with amino, (alkyl)amino, (dialkyl)amino, or loweralkoxy, lower alkyl, and lower alkyl substituted with hydroxyl, loweralkoxy, amino, (alkyl)amino, or (dialkyl)amino.

In some embodiments, L₁ is —O—, L₂ is —(CR₇R₈)_(m)— and R₂ is phenyl,pyridine-2-yl, pyridine-3-yl, pyrazin-2-yl, pyrimidine-5-yl,1H-imidazol-4-yl, 1H-imidazol-2-yl, or 1H-pyrazol-4-yl, each of which isoptionally substituted with one or two groups independent chosen fromlower alkyl, hydroxyl, lower alkoxy, lower alkoxy substituted withamino, (alkyl)amino, (dialkyl)amino, or lower alkoxy, lower alkyl, andlower alkyl substituted with hydroxyl, lower alkoxy, amino,(alkyl)amino, or (dialkyl)amino.

In some embodiments, L₁ is —NR₃— and L₂ is —C(O)— or —(CR₇R₈)_(m)—. Insome embodiments, L₁ is —NR₃— and L₂ is —C(O)—. In some embodiments, R₃is hydrogen.

In some embodiments, L₁ is —NR₃—, L₂ is —C(O)— or —(CR₇R₈)_(m)— and R₂is phenyl, pyridine-3-yl, or pyrazin-2-yl, each of which is optionallysubstituted with lower alkyl, hydroxyl or lower alkoxy.

In some embodiments, L₁ is —NR₃—, L₂ is —C(O)— or —(CR₇R₈)_(m)— and R₂is phenyl, pyridine-3-yl, or pyrazin-2-yl, each of which is optionallysubstituted with lower alkoxy.

In some embodiments, L₁ is —NR₃—, L₂ is —C(O)— and R₂ is phenyl,pyridine-3-yl, or pyrazin-2-yl, each of which is optionally substitutedwith lower alkoxy.

In some embodiments, L₁ is —NR₃— and L₂ is —(CR₇R₈)_(m) where m is 1. Insome embodiments, R₃ is hydrogen.

In some embodiments, L₁ is —NR₃—, L₂ is —(CR₇R₈)_(m) where m is 1, andR₂ is phenyl or phenyl substituted with lower alkoxy.

In some embodiments, L₁ is —NR₃— and L₂ is —(CR₇R₈)_(m) where m is 0. Insome embodiments, R₃ is hydrogen.

In some embodiments, L₁ is —NR₃—, L₂ is —(CR₇R₈)_(m) where m is 0, andR₂ is phenyl, [1,2,4]triazolo[4,3-a]pyridin-3-yl, pyrimidin-4-yl, orpyrimidin-2-yl, each of which is optionally substituted with loweralkoxy.

In some embodiments, L₁ is absent and L₂ is absent.

In some embodiments, L₁ is absent, L₂ is absent, and R₂ is phenyl,pyrimidin-2-yl, pyridazin-3-yl, pyrazin-2-yl, piperazin-1-yl,1H-pyrazol-4-yl, 1,2,3,4-tetrahydroisoquinolin-1-one-2-yl,2,3-dihydro-1H-isoindol-1-one-2-yl, 1,2-dihydroisoquinolin-1-one-2-yl,or 5H,6H,7H-pyrrolo[3,4-b]pyridine-7-one-2-yl, each of which isoptionally substituted with one or two groups independently chosen from5-methoxypyrimidin-2-yl, hydroxyl and lower alkoxy.

In some embodiments, L₁ taken together with L₂ is —CH═CH— or —C≡C—.

In some embodiments, L₁ taken together with L₂ is —CH═CH— or —C≡C—, andR₂ is phenyl or pyridine-3-yl, each of which is optionally substitutedwith one or two groups independently chosen from hydroxyl and loweralkoxy.

In some embodiments, L₁ taken together with L₂ is heterocyclylene. Insome embodiments, L₁ taken together with L₂ is piperazin-1,4-diyl. Insome embodiments, L₁ taken together with L₂ is heterocyclylene and R₂ ispyrimidin-2-yl, optionally substituted with one or two groupsindependently chosen from hydroxyl and lower alkoxy. In someembodiments, L₁ taken together with L₂ is piperazin-1,4-diyl and R₂ ispyrimidin-2-yl, optionally substituted with one or two groupsindependently chosen from hydroxyl and lower alkoxy

In some embodiments, L₁ is —(CR₇R₈)_(m)— and L₂ is —NR₃—, —C(O)— or —O—.

In some embodiments, L₁ is —(CR₇R₈)_(m)—, L₂ is —NR₃—, —C(O)— or —O—,and R₂ is pyridin-2-yl or pyridin-2-yl substituted with lower alkoxy.

In some embodiments, m is 1 and each occurrence of R₇ and R₈ ishydrogen.

In some embodiments, m is 2 and each occurrence of R₇ and R₈ ishydrogen.

In some embodiments, m is 1, R₇ is hydroxyl, trifluoromethyl, or loweralkyl and R₈ is hydrogen.

In some embodiments, m is 2, one occurrence of R₇ is hydroxyl,trifluoromethyl, or lower alkyl, and the other occurrence of R₇ and eachoccurrence of R₈ is hydrogen.

Also provided is a compound of Formula I chosen from

-   tert-butyl    4-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]piperazine-1-carboxylate;-   4-methoxy-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]benzamide;-   4-methoxy-N-[2-(pyridin-4-yl)-1,3-benzoxazol-5-yl]benzamide;-   N-[(4-methoxyphenyl)methyl]-2-(pyridin-3-yl)-1,3-benzoxazol-5-amine;-   2-(3-bromopyridin-4-yl)-6-[2-(morpholin-4-yl)ethoxy]-1,3-benzothiazole;-   5-methoxy-N-[2-(3-methylphenyl)-1,3-benzoxazol-5-yl]pyridine-2-carboxamide;-   6-methoxy-N-[2-(3-methylphenyl)-1,3-benzoxazol-5-yl]pyridine-3-carboxamide;-   2-methoxy-N-[2-(3-methylphenyl)-1,3-benzoxazol-5-yl]pyrimidine-5-carboxamide;-   5-methoxy-N-[2-(3-methylphenyl)-1,3-benzoxazol-5-yl]pyrazine-2-carboxamide;-   4-methoxy-N-[2-(3-methylphenyl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]benzamide;-   5-(4-methoxyphenyl)-2-(pyridin-3-yl)-1,3-benzoxazole;-   N-(4-methoxyphenyl)-2-(pyridin-3-yl)-1,3-benzoxazol-5-amine;-   2-(pyridin-3-yl)-N-{[1,2,4]triazolo[4,3-a]pyridin-3-yl}-1,3-benzoxazol-5-amine;-   2-(pyridin-3-yl)-N-(pyrimidin-4-yl)-1,3-benzoxazol-5-amine;-   2-(pyridin-3-yl)-N-(pyrimidin-2-yl)-1,3-benzoxazol-5-amine;-   5-(5-methoxypyridin-2-yl)-2-(pyridin-3-yl)-1,3-benzoxazole;-   5-(2-methoxypyrimidin-5-yl)-2-(pyridin-3-yl)-1,3-benzoxazole;-   5-(5-methoxypyrimidin-2-yl)-2-(pyridin-3-yl)-1,3-benzoxazole;-   5-(6-methoxypyridazin-3-yl)-2-(pyridin-3-yl)-1,3-benzoxazole;-   5-(5-methoxypyrazin-2-yl)-2-(pyridin-3-yl)-1,3-benzoxazole;-   1-methyl-4-[5-(pyrimidin-5-ylmethoxy)-1-benzofuran-2-yl]-1H-pyrazole-3-carbonitrile;-   4-[5-(pyrimidin-5-ylmethoxy)-1-benzofuran-2-yl]pyridine-3-carbonitrile;-   4-{5-[(5-methoxypyridin-2-yl)methoxy]-1-benzofuran-2-yl}pyridine-3-carbonitrile;-   4-{5-[(5-methoxypyridin-2-yl)methoxy]-1-benzofuran-2-yl}pyridine;-   4-{5-[(1-methyl-1H-imidazol-4-yl)methoxy]-1-benzofuran-2-yl}pyridine-3-carbonitrile;-   4-{5-[(1-methyl-1H-imidazol-2-yl)methoxy]-1-benzofuran-2-yl}pyridine-3-carbonitrile;-   5-methoxy-2-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]-2,3-dihydro-1H-isoindol-1-one;-   3-{6-[(E)-2-(4-methoxyphenyl)ethenyl]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine;-   4-[5-(pyridin-3-yloxy)-1-benzofuran-2-yl]pyridine-3-carbonitrile;-   6-methoxy-2-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]-1,2,3,4-tetrahydroisoquinolin-1-one;-   dimethyl({3-[4-({[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)phenoxy]propyl})amine;-   5-[(1-methyl-1H-pyrazol-4-yl)methoxy]-2-(pyridin-3-yl)-1,3-benzoxazole;-   5-[(4-methoxyphenyl)methoxy]-2-(pyridin-3-yl)-1,3-benzoxazole;-   5-[(3-methoxyphenyl)methoxy]-2-(pyridin-3-yl)-1,3-benzoxazole;-   5-[(5-methoxypyridin-2-yl)methoxy]-2-(pyridin-3-yl)-1,3-benzoxazole;-   2-(pyridin-3-yl)-5-(pyridin-3-ylmethoxy)-1,3-benzoxazole;-   5-{5H,6H-imidazo[2,1-b][1,3]thiazol-3-ylmethoxy}-2-(pyridin-3-yl)-1,3-benzoxazole;-   1-(pyridin-2-yl)-2-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]ethan-1-ol;-   1-(pyridin-2-yl)-2-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]ethan-1-one;-   6-methoxy-2-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]-1,2-dihydroisoquinolin-1-one;-   2-(pyridin-3-yl)-N-[2,2,2-trifluoro-1-(4-methoxyphenyl)ethyl]-[1,3]oxazolo[5,4-b]pyridin-6-amine;-   3-{6-[2-(4-methoxyphenyl)ethynyl]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine;-   3-{6-[(Z)-2-(4-methoxyphenyl)ethenyl]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine;-   5-methoxy-2-[2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]-2,3-dihydro-1H-isoindol-1-one;-   5-[(5-methoxypyrazin-2-yl)methoxy]-2-(pyridin-3-yl)-1,3-benzoxazole;-   3-methoxy-6-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]-5H,6H,7H-pyrrolo[3,4-b]pyridin-7-one;-   2-(pyridin-3-yl)-6-(pyridin-3-ylmethoxy)-1,3-benzoxazole;-   3-{6-[2-(pyridin-3-yl)ethynyl]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine;-   5-{[(5-methoxypyridin-2-yl)oxy]methyl}-2-(pyridin-3-yl)-1,3-benzoxazole;-   4-[5-(pyridin-3-ylmethoxy)-1-benzofuran-2-yl]pyridine-3-carbonitrile;-   4-{5-[(1-methyl-1H-pyrazol-4-yl)methoxy]-1-benzofuran-2-yl}pyridine-3-carbonitrile;-   3-[5-(pyridin-3-ylmethoxy)-1-benzofuran-2-yl]pyridine-4-carbonitrile;-   3-{5-[(1-methyl-1H-pyrazol-4-yl)methoxy]-1-benzofuran-2-yl}pyridine-4-carbonitrile;-   3-{6-[1-(5-methoxypyridin-2-yl)ethoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine;-   4-{5-[(5-methoxypyrazin-2-yl)methoxy]-1-benzofuran-2-yl}pyridine-3-carbonitrile;-   6-({[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)pyridin-3-ol;-   5-{[5-(prop-2-en-1-yloxy)pyrazin-2-yl]methoxy}-2-(pyridin-3-yl)-1,3-benzoxazole;-   5-({[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)-1,2-dihydropyrazin-2-one;-   1-methyl-5-({[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)-1,2-dihydropyrazin-2-one;-   5-[4-(5-methoxypyrimidin-2-yl)piperazin-1-yl]-2-(pyridin-3-yl)-1,3-benzoxazole;-   3-{6-[(5-methoxypyridin-2-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine;-   5-(1-methyl-1H-pyrazol-4-yl)-2-(pyridin-3-yl)-1,3-benzoxazole;-   3-{6-[(6-methoxypyridin-3-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine;-   5-[(5-methoxypyridin-2-yl)methoxy]-2-(pyridin-4-yl)-1,3-benzoxazole;-   [(3-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}phenyl)methyl]dimethylamine;-   5-[(5-methoxypyridin-2-yl)methoxy]-2-(1-methyl-1H-pyrazol-4-yl)-1,3-benzoxazole;-   5-[(5-methoxypyridin-2-yl)methoxy]-2-(pyrazin-2-yl)-1,3-benzoxazole;-   5-[(5-methoxypyridin-2-yl)methoxy]-2-(1-methylpiperidin-4-yl)-1,3-benzoxazole;-   5-[(5-methoxypyridin-2-yl)methoxy]-2-(1,3-thiazol-5-yl)-1,3-benzoxazole;-   5-[2-(pyridin-2-yloxy)ethoxy]-2-(pyridin-3-yl)-1,3-benzoxazole;-   4-[5-(1H-pyrazol-4-ylmethoxy)-1-benzofuran-2-yl]pyridine-3-carbonitrile;-   3-{[(2-{5H,6H-imidazo[2,1-b][1,3]thiazol-3-yl}-1-benzofuran-5-yl)oxy]methyl}pyridine;-   2-(3-fluoroazetidin-1-yl)-5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazole;-   2-{3H,4H,5H,6H,7H-imidazo[4,5-c]pyridin-5-yl}-5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazole;-   5-[(5-methoxypyridin-2-yl)methoxy]-2-{2H,4H,5H,6H,7H-pyrazolo[4,3-c]pyridin-5-yl}-1,3-benzoxazole;-   2-{5H,6H,7H,8H-imidazo[1,5-a]pyrazin-7-yl}-5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazole;-   5-[(5-methoxypyridin-2-yl)methoxy]-2-{5H,    6H,7H-pyrrolo[3,4-b]pyridin-6-yl}-1,3-benzoxazole;-   7-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-5,6,7,8-tetrahydro-1,7-naphthyridine;-   2-(1H-imidazol-1-yl)-5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazole;-   2-{5H,6H,7H,8H-imidazo[1,2-a]pyrazin-7-yl}-5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazole;-   4-(5-{[1-(2-methoxyethyl)-1H-pyrazol-4-yl]methoxy}-1-benzofuran-2-yl)pyridine-3-carbonitrile;-   2-[5-(2-methoxyethoxy)pyridin-3-yl]-5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazole;-   N-(5-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}pyridin-2-yl)acetamide;-   5-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}pyridin-2-amine;-   methyl({[4-({[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)phenyl]methyl})amine;-   4-(5-{[1-(2-hydroxyethyl)-1H-pyrazol-4-yl]methoxy}-1-benzofuran-2-yl)pyridine-3-carbonitrile;-   dimethyl({2-[4-({[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)phenoxy]ethyl})amine;-   5-{[5-(2-methoxyethoxy)pyridin-2-yl]methoxy}-2-(pyridin-3-yl)-1,3-benzoxazole;-   4-[5-({1-[2-(dimethylamino)ethyl]-1H-pyrazol-4-yl}methoxy)-1-benzofuran-2-yl]pyridine-3-carbonitrile;-   5-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-N-methylpyridin-2-amine;-   3-{[(2-{2-bromo-5H,6H-imidazo[2,1-b][1,3]thiazol-3-yl}-1-benzofuran-5-yl)oxy]methyl}pyridine;-   5-[(5-methoxypyrazin-2-yl)methoxy]-1-methyl-2-(pyridin-3-yl)-1H-1,3-benzodiazole;-   6-[(5-methoxypyrazin-2-yl)methoxy]-1-methyl-2-(pyridin-3-yl)-1H-1,3-benzodiazole;-   5-[(5-methoxypyrazin-2-yl)methoxy]-2-(pyridin-3-yl)-1H-1,3-benzodiazole;-   5-[(5-methoxypyridin-2-yl)methoxy]-2-(piperazin-1-yl)-1,3-benzoxazole;-   N-methyl-6-({[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)pyridin-3-amine;-   3-[5-(pyridin-3-ylmethoxy)-1-benzofuran-2-yl]-5H,6H-imidazo[2,1-b][1,3]thiazole-2-carbonitrile;-   5-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-N-methylpyridine-2-carboxamide;-   5-[(5-methoxypyridin-2-yl)methoxy]-2-(1-methyl-1H-imidazol-4-yl)-1,3-benzoxazole;-   5-methoxy-N-{[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]methyl}pyridin-2-amine;-   4-(5-{5H,6H-imidazo[2,1-b][1,3]thiazol-3-ylmethoxy}-1-benzofuran-2-yl)pyridine-3-carbonitrile;-   5-({5-[2-(morpholin-4-yl)ethoxy]pyridin-2-yl}methoxy)-2-(pyridin-3-yl)-1,3-benzoxazole;-   2-bromo-6-{5-[(5-methoxypyridin-2-yl)methoxy]-1-benzofuran-2-yl}benzonitrile;-   4-{[2-(4-chlorophenyl)-1,3-benzoxazol-5-yl]carbamoyl}phenyl acetate;-   N-(2-phenyl-1,3-benzoxazol-5-yl)benzamide;-   4-methoxy-N-[2-(3-methylphenyl)-1,3-benzoxazol-5-yl]benzamide;-   2-methoxy-N-[2-(4-methoxyphenyl)-1,3-benzoxazol-5-yl]benzamide;-   4-methoxy-N-[2-(4-methoxyphenyl)-1,3-benzoxazol-5-yl]benzamide;-   3-methoxy-N-[2-(4-methoxyphenyl)-1,3-benzoxazol-5-yl]benzamide;-   3-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}pyridin-1-ium-1-olate;-   2-phenoxy-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]acetamide;-   N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]-1-benzofuran-2-carboxamide;-   N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]-6-(trifluoromethyl)pyridine-3-carboxamide;-   N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]quinoxaline-2-carboxamide;-   6-phenoxy-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]pyridine-3-carboxamide;-   N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]-2H-1,3-benzodioxole-5-carboxamide;-   3-(benzyloxy)-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]benzamide;-   3-phenoxy-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]benzamide;-   N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]quinoline-2-carboxamide;-   N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]-2,3-dihydro-1-benzofuran-2-carboxamide;-   5-methyl-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]pyridine-3-carboxamide;-   N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]quinoxaline-6-carboxamide;-   (2E)-3-(4-methoxyphenyl)-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]prop-2-enamide;-   5-methoxy-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]pyridine-2-carboxamide;-   3-cyano-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]benzamide;-   4-(methylsulfanyl)-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]benzamide;-   benzyl N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]carbamate;-   5-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]pyrazin-2-ol;-   5-[(5-methoxypyridin-2-yl)methoxy]-2-(pyrimidin-5-yl)-1,3-benzoxazole;-   2-(2,3-dihydro-1-benzofuran-2-yl)-5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazole;-   2-[(2R)-2,3-dihydro-1-benzofuran-2-yl]-5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazole;-   2-[(2S)-2,3-dihydro-1-benzofuran-2-yl]-5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazole;-   5-[5-(2-methoxyethoxy)pyrimidin-2-yl]-2-(pyridin-3-yl)-1,3-benzoxazole;-   5-[(5-methoxypyridin-2-yl)methoxy]-2-(5-methylpyridin-3-yl)-1,3-benzoxazole;-   5-[(5-methoxypyridin-2-yl)methoxy]-2-(2-methylpyridin-4-yl)-1,3-benzoxazole;-   5-[(5-methoxypyridin-2-yl)methoxy]-2-(3-phenoxyphenyl)-1,3-benzoxazole;-   6-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-2-methyl-2,3-dihydropyridazin-3-one;-   5-[(5-methoxypyridin-2-yl)methoxy]-2-(pyridazin-3-yl)-1,3-benzoxazole;-   5-[(5-methoxypyridin-2-yl)methoxy]-2-(pyridazin-4-yl)-1,3-benzoxazole;-   5-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-1,2-dihydropyridin-2-one;-   5-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-1-methyl-1,2-dihydropyridin-2-one;-   5-phenyl-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]-1,3,4-oxadiazole-2-carboxamide;-   5-[(5-methoxypyridin-2-yl)methoxy]-2-(pyrimidin-4-yl)-1,3-benzoxazole;-   5-[(5-bromopyridin-2-yl)methoxy]-2-(pyridin-3-yl)-1,3-benzoxazole;-   5-(pyridin-2-ylmethoxy)-2-(pyridin-3-yl)-1,3-benzoxazole;-   N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]-1-benzofuran-5-carboxamide;-   2-phenyl-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]pyrimidine-5-carboxamide;-   N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]-4-(pyrimidin-2-yl)benzamide;-   1-methyl-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]-1H-pyrazole-4-carboxamide;-   4-[(6-methylpyrazin-2-yl)oxy]-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]benzamide;-   4-(phenoxymethyl)-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]benzamide;-   2-phenoxy-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]pyridine-3-carboxamide;-   4-cyano-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]benzamide;-   6-methoxy-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]pyridine-2-carboxamide;-   2-methyl-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]pyridine-4-carboxamide;-   3-methoxy-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]pyridine-2-carboxamide;-   4-methoxy-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]pyridine-2-carboxamide;-   4-hydroxy-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]pyridine-2-carboxamide;-   3-methoxy-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]-1,2-oxazole-5-carboxamide;-   5-methoxy-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]pyridine-3-carboxamide;-   6-({[2-(1-methyl-1H-pyrazol-4-yl)-1,3-benzoxazol-5-yl]oxy}methyl)pyridin-3-ol;-   5-[(5-methoxypyrazin-2-yl)methoxy]-2-(1-methyl-1H-pyrazol-4-yl)-1,3-benzoxazole;-   2-methoxy-5-({[2-(1-methyl-1H-pyrazol-4-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)pyrazine;-   3-{6-[(5-bromopyridin-2-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine;-   3-methoxy-6-({[2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)pyridazine;-   3-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}benzonitrile;-   4-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}benzonitrile;-   5-(1-methyl-1H-pyrazol-4-yl)-2-({[2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)pyridine;-   3-methoxy-5-({[2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)pyridine;-   4-methoxy-2-({[2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)pyridine;-   2-({[2-(1-methyl-1H-pyrazol-4-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)pyrazine;-   [(3-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}phenyl)methyl](methyl)amine;-   (5-methoxypyridin-2-yl)methyl    N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]carbamate;-   2-(5-methoxypyridin-2-yl)-5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazole;-   2-(1-benzofuran-2-yl)-5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazole;-   5-[(5-methoxypyridin-2-yl)methoxy]-2-[6-(trifluoromethyl)pyridin-3-yl]-1,3-benzoxazole;-   2-(1-benzofuran-5-yl)-5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazole;-   2-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}quinoline;-   2-[3-(benzyloxy)phenyl]-5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazole;-   5-[(5-methoxypyridin-2-yl)methoxy]-2-[4-(pyrimidin-2-yl)phenyl]-1,3-benzoxazole;-   2-[(E)-2-(4-Methoxyphenyl)ethenyl]-5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazole;-   5-methoxy-2-({[2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)pyrimidine;-   6-({[2-(1-methyl-1H-pyrazol-4-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)pyridin-3-amine;-   5-{5-[(5-hydroxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-N-methylpyridine-2-carboxamide;-   6-{6-[(5-methoxypyridin-2-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}-2-methyl-2,3-dihydropyridazin-3-one;-   2-methyl-6-({[2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)-2,3-dihydropyridazin-3-one;-   2-{6-[(5-methoxypyridin-2-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyrazine;-   5-{6-[(5-methoxypyridin-2-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}-N-methylpyridine-2-carboxamide;-   5-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-1-methyl-1,2-dihydropyrazin-2-one;-   6-(6-{[5-(2-fluoroethoxy)pyridin-2-yl]methoxy}-[1,3]oxazolo[5,4-b]pyridin-2-yl)-2-methyl-2,3-dihydropyridazin-3-one;-   5-methoxy-2-({[2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)pyridin-1-ium-1-olate;-   3-{6-[(5-methoxy-1-oxidopyridin-1-ium-2-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridin-1-ium-1-olate;-   5-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-2-(methylcarbamoyl)pyridin-1-ium-1-olate;-   (5-hydroxypyridin-2-yl)methyl    N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]carbamate;-   5-methoxy-N-[2-(1-methyl-6-oxo-1,6-dihydropyridazin-3-yl)-1,3-benzoxazol-5-yl]pyridine-2-carboxamide;-   5-methoxy-N-[2-(1-methyl-6-oxo-1,6-dihydropyridazin-3-yl)-1,3-benzoxazol-5-yl]pyridine-3-carboxamide;-   4-methoxy-N-[2-(1-methyl-6-oxo-1,6-dihydropyridazin-3-yl)-1,3-benzoxazol-5-yl]pyridine-2-carboxamide;-   1-methyl-N-[2-(1-methyl-6-oxo-1,6-dihydropyridazin-3-yl)-1,3-benzoxazol-5-yl]-6-oxo-1,6-dihydropyridazine-3-carboxamide;-   [(5-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}pyridin-3-yl)methyl](methyl)amine;-   6-{5-[(5-hydroxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-2-methyl-2,3-dihydropyridazin-3-one;    and-   N-(5-Methoxypyridin-3-yl)-2-(pyridin-3-yl)-1,3-benzoxazole-5-carboxamide;    or a pharmaceutically acceptable salt thereof, wherein the compound    of Formula I, or a pharmaceutically acceptable salt there of, is    labeled with one or more positron-emitting radionuclides.

Also provided is a compound of Formula I chosen from

-   tert-butyl    4-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]piperazine-1-carboxylate;-   4-methoxy-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]benzamide;-   4-methoxy-N-[2-(pyridin-4-yl)-1,3-benzoxazol-5-yl]benzamide;-   N-[(4-methoxyphenyl)methyl]-2-(pyridin-3-yl)-1,3-benzoxazol-5-amine;-   2-(3-bromopyridin-4-yl)-6-[2-(morpholin-4-yl)ethoxy]-1,3-benzothiazole;-   5-methoxy-N-[2-(3-methylphenyl)-1,3-benzoxazol-5-yl]pyridine-2-carboxamide;-   6-methoxy-N-[2-(3-methylphenyl)-1,3-benzoxazol-5-yl]pyridine-3-carboxamide;-   2-methoxy-N-[2-(3-methylphenyl)-1,3-benzoxazol-5-yl]pyrimidine-5-carboxamide;-   5-methoxy-N-[2-(3-methylphenyl)-1,3-benzoxazol-5-yl]pyrazine-2-carboxamide;-   4-methoxy-N-[2-(3-methylphenyl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]benzamide;-   5-(4-methoxyphenyl)-2-(pyridin-3-yl)-1,3-benzoxazole;-   N-(4-methoxyphenyl)-2-(pyridin-3-yl)-1,3-benzoxazol-5-amine;-   2-(pyridin-3-yl)-N-{[1,2,4]triazolo[4,3-a]pyridin-3-yl}-1,3-benzoxazol-5-amine;-   2-(pyridin-3-yl)-N-(pyrimidin-4-yl)-1,3-benzoxazol-5-amine;-   2-(pyridin-3-yl)-N-(pyrimidin-2-yl)-1,3-benzoxazol-5-amine;-   5-(5-methoxypyridin-2-yl)-2-(pyridin-3-yl)-1,3-benzoxazole;-   5-(2-methoxypyrimidin-5-yl)-2-(pyridin-3-yl)-1,3-benzoxazole;-   5-(5-methoxypyrimidin-2-yl)-2-(pyridin-3-yl)-1,3-benzoxazole;-   5-(6-methoxypyridazin-3-yl)-2-(pyridin-3-yl)-1,3-benzoxazole;-   5-(5-methoxypyrazin-2-yl)-2-(pyridin-3-yl)-1,3-benzoxazole;-   1-methyl-4-[5-(pyrimidin-5-ylmethoxy)-1-benzofuran-2-yl]-1H-pyrazole-3-carbonitrile;-   4-[5-(pyrimidin-5-ylmethoxy)-1-benzofuran-2-yl]pyridine-3-carbonitrile;-   4-{5-[(5-methoxypyridin-2-yl)methoxy]-1-benzofuran-2-yl}pyridine-3-carbonitrile;-   4-{5-[(5-methoxypyridin-2-yl)methoxy]-1-benzofuran-2-yl}pyridine;-   4-{5-[(1-methyl-1H-imidazol-4-yl)methoxy]-1-benzofuran-2-yl}pyridine-3-carbonitrile;-   4-{5-[(1-methyl-1H-imidazol-2-yl)methoxy]-1-benzofuran-2-yl}pyridine-3-carbonitrile;-   5-methoxy-2-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]-2,3-dihydro-1H-isoindol-1-one;-   3-{6-[(E)-2-(4-methoxyphenyl)ethenyl]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine;-   4-[5-(pyridin-3-yloxy)-1-benzofuran-2-yl]pyridine-3-carbonitrile;-   6-methoxy-2-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]-1,2,3,4-tetrahydroisoquinolin-1-one;-   dimethyl({3-[4-({[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)phenoxy]propyl})amine;-   5-[(1-methyl-1H-pyrazol-4-yl)methoxy]-2-(pyridin-3-yl)-1,3-benzoxazole;-   5-[(4-methoxyphenyl)methoxy]-2-(pyridin-3-yl)-1,3-benzoxazole;-   5-[(3-methoxyphenyl)methoxy]-2-(pyridin-3-yl)-1,3-benzoxazole;-   5-[(5-methoxypyridin-2-yl)methoxy]-2-(pyridin-3-yl)-1,3-benzoxazole;-   2-(pyridin-3-yl)-5-(pyridin-3-ylmethoxy)-1,3-benzoxazole;-   5-{5H,6H-imidazo[2,1-b][1,3]thiazol-3-ylmethoxy}-2-(pyridin-3-yl)-1,3-benzoxazole;-   1-(pyridin-2-yl)-2-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]ethan-1-ol;-   1-(pyridin-2-yl)-2-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]ethan-1-one;-   6-methoxy-2-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]-1,2-dihydroisoquinolin-1-one;-   2-(pyridin-3-yl)-N-[2,2,2-trifluoro-1-(4-methoxyphenyl)ethyl]-[1,3]oxazolo[5,4-b]pyridin-6-amine;-   3-{6-[2-(4-methoxyphenyl)ethynyl]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine;-   3-{6-[(Z)-2-(4-methoxyphenyl)ethenyl]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine;-   5-methoxy-2-[2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]-2,3-dihydro-1H-isoindol-1-one;-   5-[(5-methoxypyrazin-2-yl)methoxy]-2-(pyridin-3-yl)-1,3-benzoxazole;-   3-methoxy-6-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]-5H,6H,7H-pyrrolo[3,4-b]pyridin-7-one;-   2-(pyridin-3-yl)-6-(pyridin-3-ylmethoxy)-1,3-benzoxazole;-   3-{6-[2-(pyridin-3-yl)ethynyl]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine;-   5-{[(5-methoxypyridin-2-yl)oxy]methyl}-2-(pyridin-3-yl)-1,3-benzoxazole;-   4-[5-(pyridin-3-ylmethoxy)-1-benzofuran-2-yl]pyridine-3-carbonitrile;-   4-{5-[(1-methyl-1H-pyrazol-4-yl)methoxy]-1-benzofuran-2-yl}pyridine-3-carbonitrile;-   3-[5-(pyridin-3-ylmethoxy)-1-benzofuran-2-yl]pyridine-4-carbonitrile;-   3-{5-[(1-methyl-1H-pyrazol-4-yl)methoxy]-1-benzofuran-2-yl}pyridine-4-carbonitrile;-   3-{6-[1-(5-methoxypyridin-2-yl)ethoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine;-   4-{5-[(5-methoxypyrazin-2-yl)methoxy]-1-benzofuran-2-yl}pyridine-3-carbonitrile;-   6-({[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)pyridin-3-ol;-   5-{[5-(prop-2-en-1-yloxy)pyrazin-2-yl]methoxy}-2-(pyridin-3-yl)-1,3-benzoxazole;-   5-({[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)-1,2-dihydropyrazin-2-one;-   1-methyl-5-({[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)-1,2-dihydropyrazin-2-one;-   5-{4-(5-methoxypyrimidin-2-yl)piperazin-1-yl}-2-(pyridin-3-yl)-1,3-benzoxazole;-   3-{6-[(5-methoxypyridin-2-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine;-   5-(1-methyl-1H-pyrazol-4-yl)-2-(pyridin-3-yl)-1,3-benzoxazole;-   3-{6-[(6-methoxypyridin-3-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine;-   5-[(5-methoxypyridin-2-yl)methoxy]-2-(pyridin-4-yl)-1,3-benzoxazole;-   [(3-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}phenyl)methyl]dimethylamine;-   5-[(5-methoxypyridin-2-yl)methoxy]-2-(1-methyl-1H-pyrazol-4-yl)-1,3-benzoxazole;-   5-[(5-methoxypyridin-2-yl)methoxy]-2-(pyrazin-2-yl)-1,3-benzoxazole;-   5-[(5-methoxypyridin-2-yl)methoxy]-2-(1-methylpiperidin-4-yl)-1,3-benzoxazole;-   5-[(5-methoxypyridin-2-yl)methoxy]-2-(1,3-thiazol-5-yl)-1,3-benzoxazole;-   5-[2-(pyridin-2-yloxy)ethoxy]-2-(pyridin-3-yl)-1,3-benzoxazole;-   4-[5-(1H-pyrazol-4-ylmethoxy)-1-benzofuran-2-yl]pyridine-3-carbonitrile;-   3-{[(2-{5H,6H-imidazo[2,1-b][1,3]thiazol-3-yl}-1-benzofuran-5-yl)oxy]methyl}pyridine;-   2-(3-fluoroazetidin-1-yl)-5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazole;-   2-{3H,4H,5H,6H,7H-imidazo[4,5-c]pyridin-5-yl}-5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazole;-   5-[(5-methoxypyridin-2-yl)methoxy]-2-{2H,4H,5H,6H,7H-pyrazolo[4,3-c]pyridin-5-yl}-1,3-benzoxazole;-   2-{5H,6H,7H,8H-imidazo[1,5-a]pyrazin-7-yl}-5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazole;-   5-[(5-methoxypyridin-2-yl)methoxy]-2{-5H,6H,7H-pyrrolo[3,4-b]pyridin-6-yl}-1,3-benzoxazole;-   7-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-5,6,7,8-tetrahydro-1,7-naphthyridine;-   2-(1H-imidazol-1-yl)-5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazole;-   2-{5H,6H,7H,8H-imidazo[1,2-a]pyrazin-7-yl}-5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazole;-   4-(5-{[1-(2-methoxyethyl)-1H-pyrazol-4-yl]methoxy}-1-benzofuran-2-yl)pyridine-3-carbonitrile;-   2-[5-(2-methoxyethoxy)pyridin-3-yl]-5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazole;-   N-(5-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}pyridin-2-yl)acetamide;-   5-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}pyridin-2-amine;-   methyl({[4-({[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)phenyl]methyl})amine;-   4-(5-{[1-(2-hydroxyethyl)-1H-pyrazol-4-yl]methoxy}-1-benzofuran-2-yl)pyridine-3-carbonitrile;-   dimethyl({2-[4-({[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)phenoxy]ethyl})amine;-   5-{[5-(2-methoxyethoxy)pyridin-2-yl]methoxy}-2-(pyridin-3-yl)-1,3-benzoxazole;-   4-[5-({1-[2-(dimethylamino)ethyl]-1H-pyrazol-4-yl}methoxy)-1-benzofuran-2-yl]pyridine-3-carbonitrile;-   5-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-N-methylpyridin-2-amine;-   3-{[(2-{2-bromo-5H,6H-imidazo[2,1-b][1,3]thiazol-3-yl}-1-benzofuran-5-yl)oxy]methyl}pyridine;-   5-[(5-methoxypyrazin-2-yl)methoxy]-1-methyl-2-(pyridin-3-yl)-1H-1,3-benzodiazole;-   6-[(5-methoxypyrazin-2-yl)methoxy]-1-methyl-2-(pyridin-3-yl)-1H-1,3-benzodiazole;-   5-[(5-methoxypyrazin-2-yl)methoxy]-2-(pyridin-3-yl)-1H-1,3-benzodiazole;-   5-[(5-methoxypyridin-2-yl)methoxy]-2-(piperazin-1-yl)-1,3-benzoxazole;-   N-methyl-6-({[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)pyridin-3-amine;-   3-[5-(pyridin-3-ylmethoxy)-1-benzofuran-2-yl]-5H,6H-imidazo[2,1-b][1,3]thiazole-2-carbonitrile;-   5-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-N-methylpyridine-2-carboxamide;-   5-[(5-methoxypyridin-2-yl)methoxy]-2-(1-methyl-1H-imidazol-4-yl)-1,3-benzoxazole;-   5-methoxy-N-{[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]methyl}pyridin-2-amine;-   4-(5-{5H,6H-imidazo[2,1-b][1,3]thiazol-3-ylmethoxy}-1-benzofuran-2-yl)pyridine-3-carbonitrile;-   5-({5-[2-(morpholin-4-yl)ethoxy]pyridin-2-yl}methoxy)-2-(pyridin-3-yl)-1,3-benzoxazole;-   2-bromo-6-{5-[(5-methoxypyridin-2-yl)methoxy]-1-benzofuran-2-yl}benzonitrile;-   4-{[2-(4-chlorophenyl)-1,3-benzoxazol-5-yl]carbamoyl}phenyl acetate;-   N-(2-phenyl-1,3-benzoxazol-5-yl)benzamide;-   4-methoxy-N-[2-(3-methylphenyl)-1,3-benzoxazol-5-yl]benzamide;-   2-methoxy-N-[2-(4-methoxyphenyl)-1,3-benzoxazol-5-yl]benzamide;-   4-methoxy-N-[2-(4-methoxyphenyl)-1,3-benzoxazol-5-yl]benzamide; and-   3-methoxy-N-[2-(4-methoxyphenyl)-1,3-benzoxazol-5-yl]benzamide,    or a pharmaceutically acceptable salt thereof, wherein the compound    of Formula I, or a pharmaceutically acceptable salt there of, is    labeled with one or more positron-emitting radionuclides.

The compounds of Formula I, or a pharmaceutically acceptable saltthereof are labeled with one or more positron-emitting radionuclides.Suitable positron-emitting radionuclides that may be incorporated in thecompounds of described herein, but are not limited to, ¹¹C, ¹³N, ¹⁵O,¹⁸F, ⁵²Fe, ⁶²Cu, ⁶⁴Cu, ⁶⁸Ga, ⁷⁴As, ⁸²Rb, ⁸⁹Zr, ¹²²I, and ¹²⁴I. In someembodiments, the one or more positron-emitting radionuclides areselected from: ¹¹C, ¹³N, ¹⁵O, ¹⁸F, ⁷⁶Br, and ¹²⁴I. In some embodimentsthe one or more positron-emitting radionuclides are selected from ¹¹C,¹³N, ¹⁵O, and ¹⁸F.

Non-metal radionuclides may be covalently linked to the compoundsdescribed herein by a reaction well known from the state of art. Whenthe radionuclide is a metallic positron-emitter, it is understood thatlabeling may require the use of a chelating agent. Such chelating agentsare well known from the state of the art.

A PET imaging agent may be labelled with the positron emitter ¹¹C or¹⁸F. Methods for the introduction of ¹¹C may include, but are notlimited to, alkylation with [¹¹C]iodomethane or [¹¹C]methyl triflate.Carbon-11 has a half-life of approximately 20 minutes, thus ¹¹C needs tobe generated in an on-site cyclotron, and is generally produced as[¹¹C]carbon dioxide. The [¹¹C]carbon dioxide is converted to thechemical species appropriate for the radiosynthesis (generally[¹¹C]iodomethane or the like), and the synthesis of theradiopharmaceutical is completed and used on-site in a PET imaging studyafter the appropriate radiochemical purity and specific activity havebeen determined. Typical methods of introducing ¹⁸F may include but arenot limited to displacement of a halide, tosylate, or other leavinggroup with [¹⁸F]tetrabutylamonium fluoride or [¹⁸F]potassium fluoridekryptofix-222. Fluorine-18 has a half life of approximately 110 minutes,thus synthesis of [¹⁸F] radiopharmaceuticals need not necessarly have tooccur at the site of the cyclotron nor proximal to the PET imaging studycenter. General methods for the introduction of these positron emittersare described in the literature (Miller et al., Angewandte ChemieInternational Edition, 47 (2008), 8998-9033).

Provided are methods of generating diagnostic images in an individualcomprising administering an effective amount of an imaging agentdescribed herein to an individual, and generating an image of at least apart of the individual.

Also provided are methods of generating diagnostic images in abiological sample comprising contacting the biological sample with aneffective amount of an imaging agent described herein and generating animage of the positron-emitter labeled compound associated with thebiological sample. In this method both the contacting and the generatingmay be conducted in vitro, alternatively the contacting is in vivo andthe generating in vitro.

Also provided are methods for detecting the presence or absence of aneurodegenerative pathologic process associated with huntingtin protein(HTT protein) in an individual comprising: administering an effectiveamount of a positron-emitter labeled compound described herein;generating an image to detect the presence or absence of HTT proteinaggregates in the brain of the individual; and detecting the presence orabsence of the pathologic process. In some embodiments, the HTT proteinaggregates are present in the basal ganglia of the brain of theindividual. In some embodiments, the pathologic process is Huntington'sdisease (HD). In some embodiments, the effective amount of the imagingagent comprises from about 0.1 to about 20 mCi. In some embodiments, theeffective amount of the imaging agent comprises about 10 mCi. In someembodiments, generating an image comprises positron emission tomography(PET) imaging, PET with concurrent computed tomography imaging (PET/CT),PET with concurrent magnetic resonance imaging (PET/MRI), or acombination thereof. In some embodiments, generating an image comprisesPET imaging.

Also provided are diagnostic methods of using the imaging agents tomonitor disease progression in a patient by quantifying the change inlevels of the target aggregates in the patient.

Also provided are methods for detecting the presence or absence of aneurodegenerative pathologic process associated with huntingtin protein(HTT protein) in an individual comprising: administering an effectiveamount of a positron-emitter labeled compound described herein;generating an image to detect the presence or absence of HTT proteinaggregates in the individual; and detecting the presence or absence ofthe pathologic process. In some embodiments, the HTT protein monomers oraggegates are present in the brain, liver, heart, or muscle of saidindividual. In some embodiments, the HTT protein aggregates are presentin the basal ganglia, cortex, hippocampus, or brain stem of the brain ofthe individual. In some embodiments, the pathologic process isHuntington's disease (HD). In some embodiments, the effective amount ofthe imaging agent comprises from about 0.1 to about 20 mCi. In someembodiments, the effective amount of the imaging agent comprises about10 mCi. In some embodiments, generating an image comprises positronemission tomography (PET) imaging, PET with concurrent computedtomography imaging (PET/CT), PET with concurrent magnetic resonanceimaging (PET/MRI), or a combination thereof. In some embodiments,generating an image comprises PET imaging.

Also provided are methods for detecting the presence or absence of aneurodegenerative pathologic process associated with β-amyloid proteinin an individual comprising: administering an effective amount of apositron-emitter labeled compound described herein; generating an imageto detect the presence or absence of β-amyloid protein aggregates in theindividual; and detecting the presence or absence of the pathologicprocess. In some embodiments, the β-amyloid protein monomers oraggegates are present in the brain, liver, heart, or muscle of saidindividual. In some embodiments, the β-amyloid protein aggregates arepresent in the basal ganglia, cortex, hippocampus, or brain stem of thebrain of the individual. In some embodiments, the pathologic process isAlzheimer's Disease (AD). In some embodiments, the effective amount ofthe imaging agent comprises from about 0.1 to about 20 mCi. In someembodiments, the effective amount of the imaging agent comprises about10 mCi. In some embodiments, generating an image comprises positronemission tomography (PET) imaging, PET with concurrent computedtomography imaging (PET/CT), PET with concurrent magnetic resonanceimaging (PET/MRI), or a combination thereof. In some embodiments,generating an image comprises PET imaging.

Provided herein are compounds having suitable HTT protein aggregate orβ-amyloid protein aggregate binding kinetics to function as efficientimaging agents for HTT protein aggregates or β-amyloid proteinaggregates. The requirements of the compounds of the invention tofunction as efficient imaging agents for HTT protein aggregates are: 1)a high affinity for HTT protein aggregates; 2) a low affinity for nearbystructures; 3) slow dissociation kinetics from HTT protein aggregates,which may conveniently be expressed as the dissociation rate constantk_(diss) as defined in the following equation, wherein A and B refer tothe HTT protein aggregate and the imaging agent, and k_(assn) is theassociation rate constant.d[AB]/dt=k _(assn)[A][B]−k _(diss)[AB]

The part of the brain most affected by HD, and thus most likely tocontain HTT protein abnormalities, is a group of nerve cells at the baseof the brain known collectively as the basal ganglia. The basal gangliaorganize muscle-driven movements of the body, or “motor movement.” Themajor components of the basal ganglia are the caudate and the putamen(together known as the striatum) and the globus pallidus (external andinternal regions). The substantia nigra and the subthalamic nucleus areoften included as part of the basal ganglia as well.

The term basal ganglia, refers to a group of subcortical nucleiresponsible primarily for motor control, as well as other roles such asmotor learning, executive functions and behaviors, and emotions.Disruption of the basal ganglia network forms the basis for severalmovement disorders. Normal function of the basal ganglia requires finetuning of neuronal excitability within each nucleus to determine theexact degree of movement facilitation or inhibition at any given moment.This is mediated by the complex organization of the striatum, where theexcitability of medium spiny neurons is controlled by several pre- andpostsynaptic mechanisms as well as interneuron activity, and secured byseveral recurrent or internal basal ganglia circuits. The motor circuitof the basal ganglia has two entry points, the striatum and thesubthalamic nucleus, and an output, the globus pallidus pars interna,which connects to the cortex via the motor thalamus.

Provided are methods for imaging part of the brain of an individualinvolving administering a positron-emitter labeled compound describedherein to the individual, e.g. into the individual's vascular system,from where it passes through the blood-brain barrier, and thengenerating an image of at least the part of the individual's brain towhich the compound has distributed.

Also provided are pharmaceutical compositions comprising an effectiveamount of a positron-emitter labeled compound described herein, or asalt thereof, together with one or more pharmaceutically-acceptableadjuvants, excipients or diluents.

An imaging agent or pharmaceutical composition thereof may beadministered to a patient in need of treatment via any suitable route.Routes of administration may include, for example, parenteraladministration (including subcutaneous, intramuscular, intravenous, bymeans of, for example a drip patch). Further suitable routes ofadministration include (but are not limited to) oral, rectal, nasal,topical (including buccal and sublingual), infusion, vaginal,intradermal, intraperitoneally, intracranially, intrathecal and epiduraladministration or administration via oral or nasal inhalation, by meansof, for example a nebulizer or inhaler, or by an implant.

An imaging agent or pharmaceutical composition thereof may also beadministered via microspheres, liposomes, other microparticulatedelivery systems or sustained release formulations placed in certaintissues including blood. Suitable examples of sustained release carriersinclude semi-permeable polymer matrices in the form of shared articles,e.g., suppositories or microcapsules. Examples of the techniques andprotocols mentioned above and other techniques and protocols which maybe used in accordance with the invention can be found in Remington'sPharmaceutical Sciences, 18th edition, Gennaro, A. R., LippincottWilliams & Wilkins; 20th edition (Dec. 15, 2000) ISBN 0-912734-04-3 andPharmaceutical Dosage Forms and Drug Delivery Systems; Ansel, N. C. etal. 7th Edition ISBN 0-683305-72-7, the entire disclosures of which areherein incorporated by reference.

Also provided are uses of positron-emitter labeled compounds describedherein for the manufacture of an imaging agent for use in a method ofdiagnosis of an individual.

Provided are methods of generating diagnostic images comprising protonemission tomography (PET). PET involves the administration of apositron-emitting radionuclide tracer to an individual. Once the tracerhas had sufficient time to associate with the target of interest, theindividual is placed within a scanning device comprising of a ring ofscintillation detectors. An emitted positron travels through theindividual's tissue for a short (isotope-dependent) distance, until itinteracts with an electron. The interaction annihilates both theelectron and the positron, producing a pair of photons moving inapproximately opposite directions. These are detected when they reach ascintillator in the scanning device. Photons that do not arrive in pairsare ignored.

Also provided are methods of generating diagnostic images comprising PETwith concurrent computed tomography imaging (PET/CT), or with concurrentmagnetic resonance imaging (PET/MRI). Computed tomography uses X-rays toshow the structure of the brain, while magnetic resonance imaging usesmagnetic fields and radio waves.

Other uses of the disclosed imaging agents and methods will becomeapparent to those skilled in the art based upon, inter alia, a review ofthis disclosure.

As will be recognized, the steps of the methods described herein neednot be performed any particular number of times or in any particularsequence. Additional objects, advantages and novel features of thedisclosure will become apparent to those skilled in the art uponexamination of the following examples thereof, which are intended to beillustrative and not intended to be limiting.

EXAMPLES

Commercially available reagents and solvents (HPLC grade) were usedwithout further purification. ¹H NMR spectra were recorded on a BrukerDRX 500 MHz spectrometer or a Bruker DPX 250 MHz spectrometer indeuterated solvents. Chemical shifts (δ) are in parts per million. SCXchromatography was performed with Biotage Isolute Flash SCX-2 loadingthe sample in methanol and eluting with methanol then 5% ammonia inmethanol.

Analytical HPLC-MS (METCR1278), was performed on Shimadzu LCMS-2010EVsystems using reverse phase Atlantis dC18 columns (3 μm, 2.1×50 mm),gradient 5-100% B (A=water/0.1% formic acid, B=acetonitrile/0.1% formicacid) over 3 minutes injection volume 3 μL, flow=1.0 mL/minute. UVspectra were recorded at 215 nm using a SPD-M20A photo diode arraydetector. Mass spectra were obtained over the range m/z 150 to 850 at asampling rate of 2 scans per second using a LCMS2010EV. Data wereintegrated and reported using Shimadzu LCMS-Solutions and PsiPortsoftware.

Analytical HPLC-MS (METCR1673), was performed on Shimadzu LCMS-2010EVsystems using reverse phase Supelco Ascentis Express (2.7 μm, 2.1×30mm), gradient 5-100% B (A=water/0.1% formic acid, B=acetonitrile/0.1%formic acid) over 1.6 minutes injection volume 3 μL, flow=1.0 mL/minute.UV spectra were recorded at 215 nm using a SPD-M20A photo diode arraydetector. Mass spectra were obtained over the range m/z 100 to 100 at asampling rate of 2 scans per second using a LCMS2010EV. Data wereintegrated and reported using Shimadzu LCMS-Solutions and PsiPortsoftware.

Alternatively, (METCR1416) analytical HPLC-MS on Shimadzu LCMS-2010EVsystems using reverse phase Water Atlantis dC18 columns (3 μm, 2.1×100mm), gradient 5-100% B (A=water/0.1% formic acid, B=acetonitrile/0.1%formic acid) over 7 minutes, injection volume 3 μL, flow=0.6 mL/minute.UV spectra were recorded at 215 nm using a SPD-M20A photo diode arraydetector. Mass spectra were obtained over the range m/z 150 to 850 at asampling rate of 2 scans per second using a LCMS2010EV. Data wereintegrated and reported using Shimadzu LCMS-Solutions and PsiPortsoftware.

Alternatively, (MET-uHPLC-AB-101) analytical HPLC-MS were performed on aWaters Acquity UPLC system with Waters PDA and ELS detectors using aPhenomenex Kinetex-XB C-18 column, (1.7 μM, 2.1 mm×100 mm at a columntemperature of 40° C., gradient 5-100% B (A=water/0.1% formic acid;B=acetonitrile/0.1% formic acid) over 5.3 minutes, then 100% B for 0.5minute, flow=0.6 mL/minute. UV spectra were recorded at 215 nm using aWaters Acquity photo diode array. Mass spectra were obtained over therange m/z 150 to 850 at a sampling rate of 5 scans per second using aWaters SQD. Data were integrated and reported using Waters MassLynx andOpenLynx software.

All example compounds display an LC purity of >95% unless statedotherwise.

Commercial Compounds

TABLE 1 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

406.82 4-{[2-(4- Chlorophenyl)-1,3- benzoxazol-5- yl]carbamoyl} phenylacetate Tr(MET-uHPLC- AB-101) = 3.89 min, (ES⁺) (M + H)⁺ 407 2

314.34 N-(2-Phenyl-1,3- benzoxazol-5- yl)benzamide Tr(MET-uHPLC- AB-101)= 3.55 min, (ES⁺) (M + H)⁺ 315 3

358.39 4-Methoxy-N-[2- (3-methylphenyl)- 1,3-benzoxazol-5- yl]benzamideTr(MET-uHPLC- AB-101) = 2.86 min, (ES⁺) (M + H)⁺ 359 4

374.39 2-Methoxy-N-[2- (4- methoxyphenyl)- 1,3-benzoxazol-5-yl]benzamide Tr(MET-uHPLC- AB-101) = 3.85 min, (ES⁺) (M + H)⁺ 375 5

374.39 4-Methoxy-N-[2- (4- methoxyphenyl)- 1,3-benzoxazol-5-yl]benzamide Tr(MET-uHPLC- AB-101) = 3.56 min, (ES⁺) (M + H)⁺ 375 6

374.39 3-Methoxy-N-[2- (4- methoxyphenyl)- 1,3-benzoxazol-5-yl]benzamide Tr(MET-uHPLC- AB-101) = 3.64 min, (ES⁺) (M + H)⁺ 375Method 1

Step 1, Method 1:4-Methoxy-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]benzamide

To a stirred solution of 2-(pyridin-3-yl)-1,3-benzoxazol-5-amine (53 mg,0.25 mmol) in pyridine (1 mL) was added 4-methoxybenzoyl chloride (41μL, 0.293 mmol) and the mixture was stirred at room temperature for 16hours. Water (10 mL) was added and the mixture stirred for 3 hours. Theprecipitate was filtered off and triturated, with sonication, in diethylether to give the title compound 63 mg (62% yield) as a beige power.

Example 1, Method1:4-Methoxy-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]benzamide

δ_(H) NMR (500 MHz, DMSO) 10.29 (s, 1H), 9.36 (d, J=1.7 Hz, 1H), 8.81(dd, J=4.8, 1.6 Hz, 1H), 8.54 (dt, J=8.0, 1.9 Hz, 1H), 8.32 (s, 1H),8.00 (d, J=8.8 Hz, 2H), 7.82-7.77 (m, 2H), 7.66 (dd, J=7.9, 4.8 Hz, 1H),7.09 (d, J=8.8 Hz, 2H), 3.85 (s, 3H). Tr(MET-uHPLC-AB-101)=2.73 min,(ES⁺) (M+H)⁺ 346.

The following examples were prepared using Method 1 described above:

TABLE 2 Mol. Ex. Structure Weight IUPAC Name LCMS data  1

345.35 4-Methoxy-N-[2- (pyridin-3-yl)-1,3- benzoxazol-5- yl]benzamideTr(MET-uHPLC- AB-101) = 2.73 min, (ES⁺) (M + H)⁺ 346  2

345.35 4-Methoxy-N-[2- (pyridin-4-yl)-1,3- benzoxazol-5- yl]benzamideTr(MET-uHPLC- AB-101) = 2.57 min, (ES⁺) (M + H)⁺ 346  3

345.36 2-Phenoxy-N-[2- (pyridin-3-yl)-1,3- benzoxazol-5- yl]acetamideTr(MET-uHPLC- AB-101) = 2.94 min, (ES⁺) (M + H)⁺ 346  4

355.35 N-[2-(Pyridin-3- yl)-1,3- benzoxazol-5-yl]- 1-benzofuran-2-carboxamide Tr(MET-uHPLC- AB-101) = 3.17 min, (ES⁺) (M + H)⁺ 356  5

384.32 N-[2-(Pyridin-3- yl)-1,3- benzoxazol-5-yl]- 6- (trifluoromethyl)pyridine-3- carboxamide Tr(MET-uHPLC- AB-101) = 2.91 min, (ES⁺) (M + H)⁺385  6

367.37 N-[2-(Pyridin-3- yl)-1,3- benzoxazol-5- yl]quinoxaline-2-carboxamide Tr(MET-uHPLC- AB-101) = 3.12 min, (ES⁺) (M + H)⁺ 368  7

408.42 6-Phenoxy-N-[2- (pyridin-3-yl)-1,3- benzoxazol-5- yl]pyridine-3-carboxamide Tr(MET-uHPLC- AB-101) = 3.23 min, (ES⁺) (M + H)⁺ 409  8

359.34 N-[2-(Pyridin-3- yl)-1,3- benzoxazol-5-yl]- 2H-1,3-benzodioxole-5- carboxamide Tr(MET-uHPLC- AB-101) = 2.73 min, (ES⁺) (M +H)⁺ 360  9

421.46 3-(Benzyloxy)-N- [2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]benzamide Tr(MET-uHPLC- AB-101) = 3.67 min, (ES⁺) (M + H)⁺ 422 10

407.43 3-Phenoxy-N-[2- (pyridin-3-yl)-1,3- benzoxazol-5- yl]benzamideTr(MET-uHPLC- AB-101) = 3.66 min, (ES⁺) (M + H)⁺ 408 11

366.38 N-[2-(Pyridin-3- yl)-1,3- benzoxazol-5- yl]quinoline-2-carboxamide Tr(MET-uHPLC- AB-101) = 3.59 min, (ES⁺) (M + H)⁺ 367 12

357.37 N-[2-(Pyridin-3- yl)-1,3- benzoxazol-5-yl]- 2,3-dihydro-1-benzofuran-2- carboxamide Tr(MET-uHPLC- AB-101) = 3.01 min, (ES⁺) (M +H)⁺ 358 13

330.35 5-Methyl-N-[2- (pyridin-3-yl)-1,3- benzoxazol-5- yl]pyridine-3-carboxamide Tr(MET-uHPLC- AB-101) = 2.01 min, (ES⁺) (M + H)⁺ 331 14

367.37 N-[2-(Pyridin-3- yl)-1,3- benzoxazol-5- yl]quinoxaline-6-carboxamide Tr(MET-uHPLC- AB-101) = 2.39 min, (ES⁺) (M + H)⁺ 368 15

371.40 (2E)-3-(4- Methoxyphenyl)- N-[2-(pyridin-3- yl)-1,3-benzoxazol-5- yl]prop-2-enamide Tr(METCR1600) = 4.11 min, (ES⁺) (M + H)⁺372 16

346.35 5-Methoxy-N-[2- (pyridin-3-yl)-1,3- benzoxazol-5- yl]pyridine-2-carboxamide Tr(MET-uHPLC- AB-101) = 2.93 min, (ES⁺) (M + H)⁺ 347 17

340.34 3-Cyano-N-[2- (pyridin-3-yl)-1,3- benzoxazol-5- yl]benzamideTr(MET-uHPLC- AB-101) = 2.72 min, (ES⁺) (M + H)⁺ 341 18

361.42 4- (Methylsulfanyl)- N-[2-(pyridin-3- yl)-1,3- benzoxazol-5-yl]benzamide Tr(MET-uHPLC- AB-101) = 3.09 min, (ES⁺) (M + H)⁺ 362 19

345.36 Benzyl N-[2- (pyridin-3-yl)-1,3- benzoxazol-5- yl]carbamateTr(MET-uHPLC- AB-101) = 3.24 min, (ES⁺) (M + H)⁺ 346Method 2

Step 1, Method 2:N-[(4-Methoxyphenyl)methyl]-2-(pyridin-3-yl)-1,3-benzoxazol-5-amine

To a stirred suspension of 2-(pyridin-3-yl)-1,3-benzoxazol-5-amine (50mg, 0.24 mmol) in 1,2-dichloroethane (1 mL), was added4-methoxybenzaldehyde (32 mg, 0.24 mmol) followed by sodiumtriacetoxyborohydride (60 mg, 0.28 mmol) and the mixture was stirred atroom temperature overnight. The mixture was treated with sodiumtriacetoxyborohydride (60 mg, 0.28 mmol) and acetic acid (0.026 mL, 0.47mmol) and stirred at 40° C. for 48 hours. The mixture was then dilutedwith ethyl acetate (20 mL), washed with water (15 mL) and saturatedsodium bicarbonate solution (15 mL). The organic extract was dried oversodium sulfate, filtered and concentrated. Purification by preparativeHPLC (acetonitrile/water) gave the title compound (13.8 mg, 18% yield)as a white solid.

Example 1, Method 2:N-[(4-Methoxyphenyl)methyl]-2-(pyridin-3-yl)-1,3-benzoxazol-5-amine

δ_(H) NMR (500 MHz, DMSO) 9.26 (dd, J=2.2, 0.6 Hz, 1H), 8.75 (dd, J=4.8,1.6 Hz, 1H), 8.44 (dt, J=8.0, 1.9 Hz, 1H), 7.61 (ddd, J=8.0, 4.8, 0.7Hz, 1H), 7.54-7.45 (m, 1H), 7.33 (d, J=8.6 Hz, 2H), 6.93-6.85 (m, 2H),6.84-6.76 (m, 2H), 6.34 (t, J=5.9 Hz, 1H), 4.24 (d, J=5.9 Hz, 2H), 3.72(s, 2H). Tr(MET-uHPLC-AB-101)=2.98 min, (ES⁺) (M+H)⁺ 332.

The following example was prepared using Method 2 described above:

TABLE 3 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

331.37 N-[(4- Methoxyphenyl) methyl]-2-(pyridin-3- yl)-1,3-benzoxazol-5- amine Tr(MET-uHPLC- AB-101) = 2.98 min, (ES⁺) (M + H)⁺ 332Method 3

Step 1, Method 3:6-Methoxy-N-[2-(3-methylphenyl)-1,3-benzoxazol-5-yl]pyridine-3-carboxamide

To a stirred suspension of 6-methoxypyridine-3-carboxylic acid (75 mg,0.49 mmol) in dichloromethane (1 mL) was added1-chloro-N,N-2-trimethylprop-1-en-1-amine (71 μL, 0.54 mmol). Themixture was stirred at room temperature for 2 hours.2-(3-Methylphenyl)-1,3-benzoxazol-5-amine (100 mg, 0.45 mmol) was thenadded followed by triethylamine (68 μL, 0.49 mmol). The mixture wasstirred at room temperature for 60 hours. Water (5 mL) was added to themixture and the organic layer was separated. The aqueous layer wasextracted twice with dichloromethane (5 mL). The organic layers werecombined and washed with saturated aqueous potassium carbonate (5 mL).Purification by FCC (silica, 0-20% ethyl acetate in dichloromethane) andtrituration with a minimum of diethyl ether to give the title compound24 mg (15% yield) as a white solid.

Example 1 Method 3:6-Methoxy-N-[2-(3-methylphenyl)-1,3-benzoxazol-5-yl]pyridine-3-carboxamide

δ_(H) NMR (500 MHz, DMSO) 10.42 (s, 1H), 8.82 (d, J=2.4 Hz, 1H), 8.27(d, J=8.4 Hz, 2H), 8.04 (s, 1H), 8.01 (d, J=7.6 Hz, 1H), 7.77 (d, J=8.8Hz, 1H), 7.73 (dd, J=8.8, 1.9 Hz, 1H), 7.51 (t, J=7.6 Hz, 1H), 7.46 (d,J=7.6 Hz, 1H), 6.98 (d, J=8.7 Hz, 1H), 3.95 (s, 3H), 2.44 (s, 3H).Tr(MET-uHPLC-AB-101)=3.68 min, (ES⁺) (M+H)⁺ 360.

The following examples were prepared using Method 3 described above:

TABLE 4 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

359.38 6-Methoxy-N-[2-(3- methylphenyl)-1,3- benzoxazol-5-yl]pyridine-3- carboxamide Tr(MET-uHPLC- AB-101) = 3.68 min, (ES⁺) (M +H)⁺ 360 2

359.38 5-Methoxy-N-[2-(3- methylphenyl)-1,3- benzoxazol-5-yl]pyridine-2- carboxamide Tr(MET-uHPLC- AB-101) = 4.09 min, (ES⁺) (M +H)⁺ 360 3

360.37 2-Methoxy-N-[2-(3- methylphenyl)-1,3- benzoxazol-5-yl]pyrimidine-5- carboxamide Tr(MET-uHPLC- AB-101) = 3.36 min, (ES⁺)(M + H)⁺ 361 4

360.37 5-Methoxy-N-[2-(3- methylphenyl)-1,3- benzoxazol-5-yl]pyrazine-2- carboxamide Tr(MET-uHPLC- AB-101) = 405 min, (ES⁺) (M +H)⁺ 361Method 4

Step 1, Method 4: N-(5-Bromo-2-chloropyridin-3-yl)-3-methylbenzamide

To a stirred solution of 5-bromo-2-chloropyridin-3-amine (500 mg, 2.41mmol) in pyridine (5 mL) at 0° C. was added 3-methylbenzoyl chloride(410 mg, 2.65 mmol). The mixture was stirred at room temperature for 1hour. Water (50 mL) was added to the mixture. The precipitate wasfiltered and washed with water to give the title compound 653 mg (83%yield) as an off-white solid. δ_(H) NMR (250 MHz, DMSO) 10.28 (s, 1H),8.49 (d, J=2.3 Hz, 1H), 8.39 (d, J=2.3 Hz, 1H), 7.85-7.70 (m, 2H), 7.45(d, J=5.2 Hz, 2H), 2.41 (s, 3H). Tr (METCR1278)=2.25 min, (ES⁺) (M+H)⁺325/327.

Step 2, Method 4: 6-Bromo-2-(3-methylphenyl)-[1,3]oxazolo[5,4-b]pyridine

To a mixture of N-(5-bromo-2-chloropyridin-3-yl)-3-methylbenzamide (200mg, 0.61 mmol), copper(I) iodide (6 mg, 0.03 mmol),N,N′-dimethylethane-1,2-diamine (7 μL, 0.06 mmol) and potassiumcarbonate (170 mg, 1.23 mmol) was added 1,4-dioxane (1 mL). The reactionwas stirred at reflux for 24 hours. The mixture was added to a dilutedaqueous solution of ammonia (100 mL). The aqueous layer was extractedwith ethyl acetate (3×100 mL). The ethyl acetate layers were combined,dried over sodium sulfate and concentrated to give the title compound120 mg (67% yield) as a beige solid. δ_(H) NMR (500 MHz, DMSO) 8.59 (d,J=2.1 Hz, 1H), 8.51 (d, J=2.1 Hz, 1H), 8.07-7.99 (m, 2H), 7.53 (q, J=7.7Hz, 2H), 2.45 (s, 3H). Tr(METCR1278)=2.58 min, (ES⁺) (M+H)⁺ 289/291.

Step 3, Method 4: 2-(3-Methylphenyl)-[1,3]oxazolo[5,4-b]pyridin-6-amine

Under nitrogen, a mixture of6-bromo-2-(3-methylphenyl)-[1,3]oxazolo[5,4-b]pyridine (230 mg, 0.8mmol), diphenylmethanimine (217 mg, 1.19 mmol),tris(dibenzylideneacetone)dipalladium(0) (44 mg, 0.05 mmol),9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphane) (41 mg, 0.07mmol) and caesium carbonate (415 mg, 1.27 mmol) in N,N-dimethylacetamide(2 mL) was stirred at 120° C. for 16 hours. The mixture was cooled toroom temperature and water (50 mL) was added. The mixture was thenextracted with ethyl acetate (3×25 mL). The combined organic layers weredried over sodium sulfate, filtered and concentrated. The residue wasdissolved in tetrahydrofuran (5 mL) and the mixture was treated with 2 Nhydrochloric acid (2 mL). The mixture was stirred at room temperaturefor 1 hour. The crude material was purified using an SCX cartridge andtriturated with diethyl ether. 20 mg of 123 mg was purified by FCC(silica, 0-5% ethyl acetate in dichloromethane) to give the titlecompound 14 mg (8% yield) as a yellow solid. δ_(H) NMR (500 MHz, DMSO)8.04-7.89 (m, 2H), 7.72 (d, J=2.5 Hz, 1H), 7.56-7.42 (m, 2H), 7.31 (d,J=2.5 Hz, 1H), 5.36 (s, 214), 2.43 (s, 3H). Tr(MET-uHPLC-AB-101)=2.54min, (ES⁺) (M+H)⁺ 226.

Step 4, Method 4:4-Methoxy-N-[2-(3-methylphenyl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]benzamide

To a stirred solution of2-(3-methylphenyl)-[1,3]oxazolo[5,4-b]pyridin-6-amine (0.249 mmol) inpyridine (1 mL) was added 4-methoxybenzoyl chloride (41 μL, 0.293 mmol)and the mixture stirred at room temperature for 16 hours. Water (10 mL)was added and the mixture was extracted with ethyl acetate (3×10 mL).The combined organic extracts were dried over sodium sulfate, filteredand concentrated. Purification by FCC (silica, 0-20% ethyl acetate indichloromethane) gave the title compound 55 mg (52% yield) as a whitepowder.

Example 1, Method 4:4-Methoxy-N-[2-(3-methylphenyl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]benzamide

δ_(H) NMR (500 MHz, DMSO) 10.47 (s, 1H), 8.67 (d, J=2.3 Hz, 1H), 8.62(d, J=2.3 Hz, 1H), 8.10-7.94 (m, 4H), 7.58-7.44 (m, 2H), 7.15-7.05 (m,2H), 3.86 (s, 3H), 2.45 (s, 3H). Tr(MET-uHPLC-AB-101)=3.64 min, (ES⁺)(M+H)⁺ 360.

The following example was prepared using Method 4 described above:

TABLE 5 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

359.38 4-Methoxy-N-[2- (3-methylphenyl)- [1,3]oxazolo[5,4- b]pyridin-6-yl]benzamide Tr(MET-uHPLC- AB-101) = 3.64 min, (ES⁺) (M + H)⁺ 360Method 5

Step 1, Method 5: 5-(4-Methoxyphenyl)-2-(pyridin-3-yl)-1,3-benzoxazole

4-Methoxyphenylboronic acid (61 mg, 0.4 mmol) and5-bromo-2-(3-pyridinyl)-1,3-benzoxazole (100 mg, 0.36 mmol) weredissolved in 1,4-dioxane (2 mL) under nitrogen in a sealed tube. 2 Msodium carbonate (0.36 mL, 0.73 mmol) was added followed bytetrakis(triphenylphosphine)palladium(0) (21 mg, 0.018 mmol) and themixture was stirred at 110° C. overnight. The mixture was cooled to roomtemperature, diluted with water (15 mL) and extracted with ethyl acetate(2×15 mL). The combined organic extracts were dried over sodium sulfate,filtered and concentrated. Purification by FCC (silica, 0-70% ethylacetate in heptane) gave the title compound 74 mg (67% yield) as a whitesolid.

Example 1, Method 5:5-(4-Methoxyphenyl)-2-(pyridin-3-yl)-1,3-benzoxazole

δ_(H) NMR (500 MHz, chloroform) 9.50 (s, 1H), 8.78 (d, J=4.0 Hz, 1H),8.54 (dt, J=8.0, 1.9 Hz, 1H), 7.94 (d, J=1.3 Hz, 1H), 7.64 (d, J=8.4 Hz,1H), 7.62-7.54 (m, 3H), 7.50 (dd, J=7.9, 4.9 Hz, 1H), 7.05-6.98 (m, 2H),3.87 (s, 3H). Tr(MET-uHPLC-AB-101)=3.58 min, (ES⁺) (M+H)⁺ 303.

The following example was prepared using Method 5 described above:

TABLE 6 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

302.33 5-(4- Methoxyphenyl)-2- (pyridin-3-yl)-1,3- benzoxazoleTr(MET-uHPLC- AB-101) = 3.58 min, (ES⁺) (M + H)⁺ 303Method 6

Step 1, Method 6:N-(4-Methoxyphenyl)-2-(pyridin-3-yl)-1,3-benzoxazol-5-amine

A pressure tube was charged with9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphane) (32 mg, 0.055mmol), tris(dibenzylideneacetone)dipalladium(0) (17 mg, 0.018 mmol) and1,4-dioxane (2 mL). The mixture was degassed using a flow of nitrogenfor 10 minutes. The mixture was then heated at 110° C. for 1 minute andcooled to room temperature. p-Anisidine (25 mg, 0.2 mmol),2-(pyridin-3-yl)-1,3-benzoxazol-5-amine (50 mg, 0.18 mmol) and caesiumcarbonate (178 mg, 0.55 mmol) were added under nitrogen and the mixturewas stirred at 110° C. overnight. The mixture was diluted with water (10mL) and extracted with ethyl acetate (2×10 mL). The combined organicextracts were dried over sodium sulfate, filtered and concentrated.Purification by preparative HPLC (acetonitrile/water) gave the titlecompound 18 mg (31% yield) as a yellow powder.

Example 1, Method 6:N-(4-Methoxyphenyl)-2-(pyridin-3-yl)-1,3-benzoxazol-5-amine

δ_(H) NMR (500 MHz, DMSO) 9.31 (d, J=1.6 Hz, 1H), 8.78 (dd, J=4.8, 1.6Hz, 1H), 8.48 (dt, J=8.0, 1.9 Hz, 1H), 7.98 (s, 1H), 7.67-7.59 (m, 2H),7.27 (d, J=2.2 Hz, 1H), 7.12-7.05 (m, 2H), 7.03 (dd, J=8.8, 2.3 Hz, 1H),6.93-6.86 (m, 2H), 3.73 (s, 3H). Tr(MET-uHPLC-AB-101)=3.17 min, (ES⁺)(M+H)⁺ 318.

The following examples were prepared using Method 6 described above:

TABLE 7 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

317.34 N-(4- Methoxyphenyl)-2- (pyridin-3-yl)-1,3- benzoxazol-5- amineTr(MET-uHPLC- AB-101) = 3.17 min, (ES⁺) (M + H)⁺ 318 2

328.33 2-(Pyridin-3-yl)-N- {[1,2,4]triazolo[4,3- a]pyridin-3-yl}-1,3-benzoxazol-5- amine Tr(MET-uHPLC- AB-101) = 1.6 min, (ES⁺) (M + H)⁺329Method 7

Step 1, Method 7:2-(Pyridin-3-yl)-N-(pyrimidin-4-yl)-1,3-benzoxazol-5-amine

4-Chloropyrimidine hydrochloride (71 mg, 0.47 mmol),2-(pyridin-3-yl)-1,3-benzoxazol-5-amine (50 mg, 0.24 mmol),diisopropylethylamine (0.12 mL, 0.71 mmol) and 2-propanol (1 mL) wereheated in a microwave at 120° C. for 3 hours. The reaction mixture wasfiltered and the filtrate was concentrated in vacuo. Purification bypreparative HPLC (acetonitrile/water) gave the title compound 7.2 mg(11% yield) as an off-white solid.

Example 1 Method 7:2-(Pyridin-3-yl)-N-(pyrimidin-4-yl)-1,3-benzoxazol-5-amine

δ_(H) NMR (500 MHz, DMSO) 9.79 (s, 1H), 9.35 (d, J=2.1 Hz, 1H), 8.81(dd, J=4.8, 1.6 Hz, 1H), 8.66 (s, 1H), 8.53 (dt, J=8.0, 1.9 Hz, 1H),8.33 (d, J=2.0 Hz, 1H), 8.29 (d, J=5.9 Hz, 1H), 7.79 (d, J=8.8 Hz, 1H),7.66 (dd, J=8.0, 4.8 Hz, 1H), 7.60 (dd, J=8.8, 2.1 Hz, 1H), 6.82 (dd,J=5.9, 1.1 Hz, 1H). Tr(MET-uHPLC-AB-101)=1.23 min, (ES⁺) (M+H)⁺ 290.

The following examples were prepared using Method 7 described above:

TABLE 8 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

289.29 2-(Pyridin-3-yl)-N- (pyrimidin-4-yl)- 1,3-benzoxazol-5- amineTr(MET-uHPLC- AB-101) = 1.23 min, (ES⁺) (M + H)⁺ 290 2

289.29 2-(Pyridin-3-yl)-N- (pyrimidin-2-yl)- 1,3-benzoxazol-5- amineTr(METCR1416 Hi res 7 min) = 2.25 min, (ES⁺) (M + H)⁺ 290Method 8

Step 1, Method 8:2-(Pyridin-3-yl)-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3-benzoxazole

A suspension of 5-bromo-2-(3-pyridinyl)-1,3-benzoxazole (200 mg, 0.73mmol), bis(pinacolato)diboron (221 mg, 0.87 mmol) and potassium acetate(214 mg, 2.18 mmol) in DMSO (4 mL) was degassed with nitrogen for 5minutes. [1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II) (27mg, 0.036 mmol) was added and the reaction was stirred at 80° C. undernitrogen for 16 hours. The reaction mixture was then cooled to roomtemperature, diluted with water (20 mL) and extracted with ethyl acetate(2×20 mL). The combined organic extracts were dried over sodium sulfate,filtered and concentrated. Purification by FCC (silica, 0-40% ethylacetate in heptane) gave the title compound 143 mg (61% yield) as awhite solid. Tr(METCR1278)=2.25 mins, (ES⁺) (M+H)⁺ 323.

Step 2, Method 8:5-(5-Methoxypyrimidin-2-yl)-2-(pyridin-3-yl)-1,3-benzoxazole

2-Chloro-5-methoxypyrimidine (69 mg, 0.48 mmol) and2-(pyridin-3-yl)-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3-benzoxazole(140 mg, 0.43 mmol) were dissolved in 1,4-dioxane (3 mL) under nitrogenin a sealed tube. 2 M sodium carbonate (0.43 mL, 0.87 mmol) was addedfollowed by tetrakis(triphenylphosphine)palladium(0) (25 mg, 0.022mmol). The reaction mixture was stirred at 110° C. overnight. Thereaction mixture was cooled to room temperature, diluted with water (20mL) and extracted with ethyl acetate (2×20 mL). The combined organiclayers were dried over sodium sulfate, filtered and concentrated.Purification by FCC (silica, 0-2% methanol in dichloromethane) gave thetitle compound 24 mg (18% yield) as a white solid.

Example 1, Method 8: (125-1)5-(5-Methoxypyrimidin-2-yl)-2-(pyridin-3-yl)-1,3-benzoxazole

δ_(H) NMR (500 MHz, DMSO) 9.38 (d, J=2.0 Hz, 1H), 8.83 (dd, J=4.8, 1.6Hz, 1H), 8.69 (s, 2H), 8.66 (d, J=1.5 Hz, 1H), 8.57 (dt, J=8.0, 1.9 Hz,1H), 8.46 (dd, J=8.6, 1.7 Hz, 1H), 7.93 (d, J=8.6 Hz, 1H), 7.67 (dd,J=7.9, 4.8 Hz, 1H), 3.98 (s, 3H). Tr(MET-uHPLC-AB-101)=2.87 min, (ES⁺)(M+H)⁺305.

The following examples were prepared using Method 8 described above:

TABLE 9 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

304.30 5-(5- Methoxypyrimidin- 2-yl)-2-(pyridin-3- yl)-1,3- benzoxazoleTr(MET-uHPLC- AB-101) = 2.87 min, (ES⁺) (M + H)⁺ 305 2

304.30 5-(6- Methoxypyridazin- 3-yl)-2-(pyridin-3- yl)-1,3- benzoxazoleTr(MET-uHPLC- AB-101) = 2.53 min, (ES⁺) (M + H)⁺ 305 3

304.30 5-(5- Methoxypyrazin-2- yl)-2-(pyridin-3- yl)-1,3- benzoxazoleTr(MET-uHPLC- AB-101) = 3.11 min, (ES⁺) (M + H)⁺ 305 4

303.31 5-(5- Methoxypyridin-2- yl)-2-(pyridin-3- yl)-1,3- benzoxazoleTr(MET-uHPLC- AB-101) = 2.02 min, (ES⁺) (M + H)⁺ 304 5

304.30 5-(2- Methoxypyrimidin- 5-yl)-2-(pyridin-3- yl)-1,3- benzoxazoleTr(MET-uHPLC- AB-101) = 2.57 min, (ES⁺) (M + H)⁺ 305Method 9

Step 1, Method 9: 5-(Methoxymethoxy)-1-benzofuran

Sodium hydride (60% in mineral oil, 579 mg, 14.48 mmol) was suspended inanhydrous N,N-dimethylformamide (25 mL) and cooled to 0° C.5-Hydroxybenzofuran (1.85 g, 13.79 mmol) dissolved inN,N-dimethylformamide (10 mL) was added slowly. The mixture was stirredunder nitrogen and warmed to room temperature over 1.5 hours. Themixture was cooled to 0° C. and chloro(methoxy)methane (1.1 mL, 14.48mmol) was added drop-wise over 30 minutes. The reaction was warmed toroom temperature and stirred for 3 hours. Water (5 mL) was added and themixture was extracted with ethyl acetate (3×50 mL). The combined organicextracts were washed with water (5×50 mL), brine (10 mL), dried overmagnesium sulfate, filtered and concentrated to give the title compound2.3 g (89% yield) as a pale yellow oil. Tr(METCR1278)=1.95 min, noionization.

Step 2, Method 9: [5-(Methoxymethoxy)-1-benzofuran-2-yl]boronic acid

5-(Methoxymethoxy)-1-benzofuran (1.00 g, 5.35 mmol) was dissolved inanhydrous tetrahydrofuran (15 mL) and cooled to −78° C. under nitrogen.1.6 M n-butyllithium in hexanes (3.51 mL, 5.62 mmol) was added drop-wiseand stirred for 1 hour at −78° C. Triisopropylborate (2.47 mL, 10.7mmol) was added drop-wise and the reaction mixture was stirred for 2hours. The reaction mixture was warmed to room temperature and stirredfor 1 hour. 2 M hydrochloric acid (16 mL) was added and the reaction wasstirred for 1 hour. The reaction mixture was diluted with water (10 mL)and extracted with tert-butyl methyl ether (3×40 mL). The combinedorganic extracts were washed with brine (10 mL), dried over magnesiumsulfate, filtered and concentrated. Purification by FCC (silica, 20-80%ethyl acetate in heptane) gave the crude title compound 374 mg (31%yield) as a beige solid which was used in the next step without furtherpurification.

Step 3, Method 9:4-[5-(Methoxymethoxy)-1-benzofuran-2-yl]pyridine-3-carbonitrile

[5-(Methoxymethoxy)-1-benzofuran-2-yl]boronic acid (374 mg, 1.68 mmol),4-bromopyridine-3-carbonitrile (339 mg, 1.85 mmol) and 2 M tripotassiumphosphate (1.7 mL) were suspended in N,N-dimethylformamide (20 mL) andsonicated under a flow of nitrogen for 5 minutes.(1R,4S)-Bicyclo[2.2.1]hept-2-yl[(1S,4R)-bicyclo[2.2.1]hept-2-yl]phosphane-chloro[2′-(dimethylamino)biphenyl-2-yl]palladium(1:1) (47 mg, 0.08 mmol) was added and the reaction was heated to 75° C.for 1.5 hours. The reaction was cooled to room temperature and thesolvents were removed in vacuo. The residue was partitioned betweenethyl acetate (50 mL) and water (20 mL), the phases were separated andthe aqueous was extracted with ethyl acetate (2×50 mL). The combinedorganic extracts were washed with brine (10 mL), dried over sodiumsulfate, filtered and concentrated. Purification by FCC (silica, 0-50%ethyl acetate in heptane) gave the title compound 254 mg (52% yield) asa pale yellow solid. Tr(MET-uHPLC-AB-101)=3.20 min, (ES⁺) (M+H)⁺ 281.

Step 4, Method 9: 4-(5-Hydroxy-1-benzofuran-2-yl)pyridine-3-carbonitrile

To a solution of4-[5-(methoxymethoxy)-1-benzofuran-2-yl]pyridine-3-carbonitrile (240 mg,0.86 mmol) in tetrahydrofuran (10 mL) was added 3 M hydrochloric acid(2.8 mL) and the mixture was stirred at 60° C. for 2 hours. The reactionmixture was cooled to room temperature and saturated aqueous sodiumbicarbonate (50 mL) and ethyl acetate (100 mL) were added. The mixturewas filtered (glass fibre filterpaper) and dried under vacuum for 2hours to give the title compound 207 mg (quantitative yield) as a yellowsolid. Tr(MET-uHPLC-AB-101)=2.41 min, (ES⁺) (M+H)⁺ 237.

Step 5, Method 9:4-{5-[(5-Methoxypyridin-2-yl)methoxy]-1-benzofuran-2-yl}pyridine-3-carbonitrile

4-(5-Hydroxy-1-benzofuran-2-yl)pyridine-3-carbonitrile (98%, 50 mg, 0.21mmol), 2-(chloromethyl)-5-methoxypyridine hydrochloride (44 mg, 0.23mmol) and potassium iodide (34 mg, 0.21 mmol) were dissolved inanhydrous N,N-dimethylformamide (2 mL) and stirred for 5 minutes at roomtemperature. Sodium hydride (60% in mineral oil, 25 mg, 0.62 mmol) wasadded and the reaction mixture was stirred under nitrogen for 15 hours.The solvents were removed in vacuo and the residue was partitionedbetween ethyl acetate (50 m) and water (20 m), the aqueous layer wasextracted with ethyl acetate (2×30 m), the combined organics were washedwith water (10 mL), brine (10 mL), dried over sodium sulfate, filtered,and concentrated. Purification by FCC (silica, 0-100% ethyl acetate inheptane) gave the title compound 34.8 mg (47% yield) as a white powder.

Example 1, Method 9:4-{5-[(5-Methoxypyridin-2-yl)methoxy]-1-benzofuran-2-yl}pyridine-3-carbonitrile

δ_(H) NMR (500 MHz, DMSO) 9.12 (s, 1H), 8.92 (d, J=5.4 Hz, 1H), 8.30 (d,J=2.9 Hz, 1H), 8.07 (d, J=5.4 Hz, 1H), 7.99-7.88 (m, 1H), 7.65 (d, J=9.0Hz, 1H), 7.52 (d, J=8.6 Hz, 1H), 7.48-7.39 (m, 2H), 7.18 (dd, J=9.0, 2.6Hz, 1H), 5.16 (s, 2H), 3.84 (s, 3H). Tr(MET-uHPLC-AB-101)=3.15 min,(ES⁺) (M+H)⁺ 358.

The following examples were prepared using Method 9 described above:

TABLE 10 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

357.36 4-{5-[(5- Methoxypyridin-2- yl)methoxy]-1- benzofuran-2-yl}pyridine-3- carbonitrile Tr(MET-uHPLC- AB-101) = 3.15 min, (ES⁺) (M +H)⁺ 358 2

332.35 4-{5-[(5- Methoxypyridin-2- yl)methoxy]-1- benzofuran-2-yl}pyridine Tr(MET-uHPLC- AB-101) = 1.92 min, (ES⁺) (M + H)⁺ 333 3

330.34 4-{5-[(1-Methyl- 1H-imidazol-4- yl)methoxy]-1- benzofuran-2-yl}pyridine-3- carbonitrile Tr(MET-uHPLC- AB-101) = 1.67 min, (ES⁺) (M +H)⁺ 331 4

330.34 4-{5-[(1-Methyl- 1H-imidazol-2- yl)methoxy]-1- benzofuran-2-yl}pyridine-3- carbonitrile Tr(MET-uHPLC- AB-101) = 1.66 min, (ES⁺) (M +H)⁺ 331.1 5

330.34 4-{5-[(1-Methyl- 1H-pyrazol-4- yl)methoxy]-1- benzofuran-2-yl}pyridine-3- carbonitrile Tr(MET-uHPLC- AB-101) = 2.94 min, (ES⁺) (M +H)⁺ 331 6

327.34 3-[5-(Pyridin-3- ylmethoxy)-1- benzofuran-2- yl]pyridine-4-carbonitrile Tr(MET-uHPLC- AB-101) = 2.24 min, (ES⁺) (M + H)⁺ 328 7

330.34 3-{5-[(1-Methyl- 1H-pyrazol-4- yl)methoxy]-1- benzofuran-2-yl}pyridine-4- carbonitrile Tr(MET-uHPLC- AB-101) = 2.95 min, (ES⁺) (M +H)⁺ 331 8

327.34 4-[5-(Pyridin-3- ylmethoxy)-1- benzofuran-2- yl]pyridine-3-carbonitrile Tr( ) = 2.22 min, (ES⁺) (M + H)⁺ 328 9

331.33 1-Methyl-4-[5- (pyrimidin-5- ylmethoxy)-1- benzofuran-2-yl]-1H-pyrazole-3- carbonitrile Tr(MET-uHPLC- AB-101) = 2.91 min, (ES⁺) (M +H)⁺ 332Method 10

Step 1, Method 10:5-Methoxy-2-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]-2,3-dihydro-1H-isoindol-1-one

Ethyl 2-(bromomethyl)-4-methoxybenzoate (100 mg, 0.37 mmol described inWO2009042907), 2-(pyridin-3-yl)-1,3-benzoxazol-5-amine (93 mg, 0.44mmol) and diisopropylethylamine (77 μL, 0.44 mmol) were dissolved inethanol (4 mL) and heated to 110° C. in a pressure tube for 18 hours.The reaction mixture was cooled to room temperature and treated with asolution of lithium hydroxide monohydrate (46 mg, 1.10 mmol) in water(0.5 mL). The reaction mixture was stirred at room temperature for 1.5hours then concentrated. Trituration in boiling ethyl acetate-ethanol(1:1 v/v) followed by recrystallisation from DMSO gave the titlecompound 5 mg (5% yield) as a yellow powder.

Example 1, Method 10:5-Methoxy-2-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]-2,3-dihydro-1H-isoindol-1-one

δ_(H) NMR (500 MHz, DMSO+5% DCl/D₂O) 9.56 (d, J=1.76 Hz, 1H), 9.18 (dt,J=1.53, 8.20 Hz, 1H), 9.10-9.04 (m, 1H), 8.35 (d, J=2.08 Hz, 1H), 8.24(dd, J=5.70, 8.09 Hz, 1H), 8.03 (dd, J=2.17, 9.00 Hz, 1H), 7.92 (d,J=9.00 Hz, 1H), 7.70 (d, J=8.43 Hz, 1H), 7.22 (d, J=1.76 Hz, 1H), 7.08(dd, J=2.16, 8.44 Hz, 1H), 5.05 (s, 2H), 3.85 (s, 3H).Tr(MET-uHPLC-AB-101)=2.88 min, (ES⁺) (M+H)⁺ 358.

The following example was prepared using Method 10 described above:

TABLE 11 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

357.36 5-Methoxy-2-[2- (pyridin-3-yl)-1,3- benzoxazol-5-yl]-2,3-dihydro-1H- isoindol-1-one Tr(MET-uHPLC- AB-101) = 2.88 min, (ES⁺)(M + H)⁺ 358Method 11

Step 1, Method 11:N-(5-Bromo-2-chloropyridin-3-yl)pyridine-3-carboxamide

To a stirred solution of 5-bromo-2-chloropyridin-3-amine (1.00 g, 4.82mmol) in pyridine (10 mL) with ice cooling, was added nicotinoylchloride hydrochloride (0.94 g, 5.30 mmol). The mixture was stirred atroom temperature for 1 hour. The mixture was concentrated, diluted withwater (60 mL) and extracted with ethyl acetate (3×60 mL). The combinedorganic extracts were dried over sodium sulfate, filtered andconcentrated to give the title compound 1.1 g as a grey solid.Filtration of the aqueous extract gave another 0.18 g of title compound,adding to 1.28 g (85% yield) as a grey powder. Tr(METCR1278)=1.57 min,(ES⁺) (M+H)⁺ 312, 314.

Step 2, Method 11: 3-{6-Bromo-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine

A pressure tube was charged withN-(5-bromo-2-chloropyridin-3-yl)pyridine-3-carboxamide (318 mg, 0.68mmol), copper(I) iodide (6.5 mg, 0.034 mmol),N,N-dimethylethane-1,2-diamine (6.0 mg, 0.068 mmol) and potassiumcarbonate (0.19 g, 1.36 mmol) in 1,4-dioxane (4 mL). The mixture wasdegassed using a flow of nitrogen for 10 minutes and heated at 110° C.for 16 hours. The mixture was then diluted with water (30 mL) andextracted with ethyl acetate (3×30 mL). The combined organic extractswere dried over sodium sulfate, filtered and concentrated. The residuewas triturated with methanol (4 mL) to give the title compound 95 mg(50% yield) as a light brown powder. Tr(METCR1278)=1.85 min, (ES⁺)(M+H)⁺ 276/278.

Step 3, Method 11:3-{6-[(E)-2-(4-Methoxyphenyl)ethenyl]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine

A pressure tube was charged with3-{6-bromo-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine (95 mg, 0.18 mmol),4-methoxystyrene (78 mg, 0.58 mmol), triphenylphosphine (15 mg, 0.058mmol) and potassium carbonate (120 mg, 0.87 mmol) inN,N-dimethylformamide (1 mL). The mixture was degassed using a flow ofnitrogen for 5 minutes then heated at 90° C. for 2 hours. The mixturewas cooled to room temperature, diluted with water (10 mL) and filteredto give a brown solid which was dried under vacuum (80 mg). The solidwas then charged in a pressure tube with 4-methoxystyrene (78 mg, 0.58mmol), triphenylphosphine (15 mg, 0.058 mmol) and potassium carbonate(120 mg, 0.87 mmol) in N,N-dimethylformamide (1 mL). The mixture wasdegassed using a flow of nitrogen for 5 minutes then heated at 90° C.for 2 hours. The mixture was then cooled to room temperature, dilutedwith water (10 mL) and filtered to give a black solid, which was washedwith ethyl acetate (2 mL). The solid was then dissolved in DMSO (2 mL),filtered and the filtrate was concentrated under reduced pressure.Purification by FCC (silica, 0-2% methanol in dichloromethane) andrecrystallisation in DMSO:acetonitrile (1:1) gave the title compound 2mg (2% yield) as a white powder.

Example 3, Method 11:3-{6-[(E)-2-(4-Methoxyphenyl)ethenyl]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine

δ_(H) NMR (500 MHz, DMSO) 9.38 (d, J=1.7 Hz, 1H), 8.85 (dd, J=4.8, 1.6Hz, 1H), 8.65-8.52 (m, 3H), 7.69 (dd, J=8.0, 4.8 Hz, 1H), 7.58 (d, J=8.7Hz, 2H), 7.44 (d, J=16.5 Hz, 1H), 7.29 (d, J=16.5 Hz, 1H), 6.99 (d,J=8.7 Hz, 2H), 3.79 (s, 3H). Tr(MET-uHPLC-AB-101)=3.54 min, (ES⁺) (M+H)⁺330.

The following example was prepared using Method 11 described above:

TABLE 12 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

329.35 3-{6-[(E)-2-(4- Methoxyphenyl) ethenyl]- [1,3]oxazolo[5,4-b]pyridin-2- yl}pyridine Tr(MET-uHPLC- AB-101) = 3.54 min, (ES⁺) (M +H)⁺ 330Method 12

Step 1, Method 12:(4-[5-(Pyridin-3-yloxy)-1-benzofuran-2-yl]pyridine-3-carbonitrile

Caesium carbonate (138 mg, 0.42 mmol),2,2,6,6-tetramethylheptane-3,5-dione (47 μL, 0.21 mmol) and copper(I)iodide (4 mg, 0.02 mmol) were dissolved in N,N-dimethylformamide (1 mL)and stirred in a screw-cap vial for 5 minutes at room temperature.4-(5-Hydroxy-1-benzofuran-2-yl)pyridine-3-carbonitrile (50 mg, 0.21mmol, prepared by Method 9) and 3-iodopyridine (46 mg, 0.22 mmol) wereadded and the reaction was sealed and heated to 60° C. for 16 hours,then to 90° C. for 24 hours. The reaction mixture was cooled to roomtemperature and the solvents removed in vacuo. The residue was sonicatedin ethyl acetate (20 mL) and passed through a pad of celite. The pad waswashed with ethyl acetate (2×20 mL). The combined organics were washedwith water (10 mL), brine (10 mL), dried over sodium sulfate, filteredand concentrated. Purification by preparative HPLC(acetonitrile/water+0.2% ammonium hydroxide) gave the title compound12.5 mg (18% yield) as a tan powder.

Example 1, Method 12:4-[5-(Pyridin-3-yloxy)-1-benzofuran-2-yl]pyridine-3-carbonitrile

δ_(H) NMR (500 MHz, DMSO) 9.14 (s, 1H), 8.95 (d, J=5.4 Hz, 1H), 8.41 (s,1H), 8.37 (dd, J=3.9, 2.1 Hz, 1H), 8.10 (d, J=5.4 Hz, 1H), 7.99 (s, 1H),7.80 (d, J=8.9 Hz, 1H), 7.59 (d, J=2.5 Hz, 1H), 7.47-7.39 (m, 2H), 7.28(dd, J=8.9, 2.6 Hz, 1H). Tr(MET-uHPLC-AB-101)=2.65 min, (ES⁺) (M+H)⁺314.

The following example was prepared using Method 12 described above:

TABLE 13 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

313.31 4-[5-(Pyridin-3- yloxy)-1- benzofuran-2- yl]pyridine-3-carbonitrile Tr(MET-uHPLC- AB-101) = 2.65 min, (ES⁺) (M + H)⁺ 314Method 13

Step 1, Method 13:6-Methoxy-2-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]-1,2,3,4-tetrahydroisoquinolin-1-one

2-(2-Chloroethyl)-4-methoxybenzoyl chloride (226 mg, 0.97 mmol,described in WO2007093366) and 2-(pyridin-3-yl)-1,3-benzoxazol-5-amine(205 mg, 0.97 mmol) were dissolved in anhydrous tetrahydrofuran (10 mL)under nitrogen. Sodium hydride (60% in mineral oil, 78 mg, 1.9 mmol) wasadded and the mixture heated to 60° C. for 2 hours. The reaction mixturewas cooled to room temperature, quenched with water (10 mL) andextracted with ethyl acetate (4×15 mL). The combined organic extractswere washed with water (15 mL) and brine (15 mL) then dried overmagnesium sulfate, filtered and concentrated. Preparative HPLC(acetonitrile/water+0.1% formic acid) gave the title compound 23 mg (5%yield) as a white powder.

Example 1, Method 13:6-Methoxy-2-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]-1,2,3,4-tetrahydroisoquinolin-1-one

δ_(H) NMR (500 MHz, DMSO) 9.37 (d, J=1.63 Hz, 1H), 8.82 (dd, J=1.59,4.81 Hz, 1H), 8.56 (dt, J=1.87, 7.99 Hz, 1H), 7.93-7.82 (m, 3H), 7.67(dd, J=4.82, 7.96 Hz, 1H), 7.50 (dd, J=2.08, 8.70 Hz, 1H), 6.97-6.91 (m,2H), 4.01 (t, J=6.46 Hz, 2H), 3.85 (s, 3H), 3.15 (t, J=6.41 Hz, 2H).Tr(MET-uHPLC-AB-101)=2.83 min, (ES⁺) (M+H)⁺ 372.

The following example was prepared using Method 13 described above:

TABLE 14 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

371.39 6-Methoxy-2-[2- (pyridin-3-yl)-1,3- benzoxazol-5-yl]- 1,2,3,4-tetrahydroisoquinol in-1-one Tr(MET-uHPLC- AB-101) = 2.83 min, (ES⁺)(M + H)⁺ 372Method 14

Step 1, Method 14: 2-(Pyridin-3-yl)-1,3-benzoxazol-5-ol

2-(Pyridin-3-yl)-1,3-benzoxazol-5-amine (350 mg, 1.66 mmol) was addedportion-wise to a stirred solution of sulphuric acid (1.76 mL, 33.14mmol) in water (5.25 mL) at room temperature. The solution was cooled to0-5° C. and a solution of sodium nitrite (126 mg, 1.82 mmol) in water(3.5 mL) was added drop-wise. The mixture was stirred for 30 minutes at0-5° C. A solution of copper(II) nitrate (20.5 g, 109.4 mmol) in water(35 mL) was added to the reaction mixture followed by copper(I) oxide(237 mg, 1.66 mmol). The mixture was shaken vigorously for 10 minutes.The mixture was then basified using saturated a solution of saturatedsodium hydrogen carbonate until pH reached 8-9. 10% Aqueous ammonia (30mL) was added and the resulting aqueous solution was extracted usingethyl acetate (2×150 mL). The combined organic extracts were dried oversodium sulfate, filtered and concentrated. Purification by FCC (silica,0-5% methanol in dichloromethane) gave the title compound 127 mg (36%yield) as a yellow powder. Tr(MET-uHPLC-AB-101)=1.77 min, (ES⁺)(M+H)⁺213.

Step 2, Method 14:5-[(4-Methoxyphenyl)methoxy]-2-(pyridin-3-yl)-1,3-benzoxazole

To sodium hydride (60% in mineral oil, 5.7 mg, 0.14 mmol) under nitrogenwas added a solution of 2-(pyridin-3-yl)-1,3-benzoxazol-5-ol (30 mg,0.14 mmol) in N,N-dimethylformamide (1 mL) and the mixture was stirredat room temperature for 30 minutes. A solution of 4-methoxybenzylbromide (28 mg, 0.14 mmol) in N,N-dimethylformamide (0.5 mL) was addedand the mixture was stirred at room temperature for 1 hour. The mixturewas quenched with water (0.5 mL), diluted with water (15 mL) andextracted with ethyl acetate (2×15 mL). The combined organic extractswere dried over sodium sulfate, filtered and concentrated. Purificationby FCC (silica, 20-100% ethyl acetate in heptane), trituration inacetonitrile (2 mL) and drying under vacuum gave the title compound 12mg (26% yield) as a white powder.

Example 1, Method 14:5-[(4-Methoxyphenyl)methoxy]-2-(pyridin-3-yl)-1,3-benzoxazole

δ_(H) NMR (500 MHz, DMSO) 9.32 (d, J=1.8 Hz, 1H), 8.80 (dd, J=4.8, 1.6Hz, 1H), 8.50 (dt, J=8.0, 1.9 Hz, 1H), 7.72 (d, J=8.9 Hz, 1H), 7.65 (dd,J=7.9, 4.8 Hz, 1H), 7.47 (d, J=2.5 Hz, 1H), 7.42 (d, J=8.6 Hz, 2H), 7.10(dd, J=8.9, 2.5 Hz, 1H), 6.96 (d, J=8.6 Hz, 2H), 5.11 (s, 2H), 3.76 (s,3H). Tr(MET-uHPLC-AB-101)=3.56 min, (ES⁺) (M+H)⁺ 333.

The following examples were prepared using Method 14 described above:

TABLE 15 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

332.35 5-[(4- Methoxyphenyl) methoxy]-2-(pyridin- 3-yl)-1,3- benzoxazoleTr(MET-uHPLC- AB-101) = 3.56 min, (ES⁺) (M + H)⁺ 333 2

332.35 5-[(3- Methoxyphenyl) methoxy]-2-(pyridin- 3-yl)-1,3- benzoxazoleTr(MET-uHPLC- AB-101) = 3.58 min, (ES⁺) (M + H)⁺ 333 3

333.34 5-[(5- Methoxypyridin-2- yl)methoxy]-2- (pyridin-3-yl)-1,3-benzoxazole Tr(MET-uHPLC- AB-101), = 2.61 min, (ES⁺) (M + H)⁺ 334 4

303.31 2-(Pyridin-3-yl)- 5-(pyridin-3- ylmethoxy)-1,3- benzoxazoleTr(MET-uHPLC- AB-101), = 1.73 min, (ES⁺) (M + H)⁺ 304 5

350.39 5-{5H,6H- Imidazo[2,1-b] [1,3]thiazol-3- ylmethoxy}-2-(pyridin-3-yl)-1,3- benzoxazole Tr(MET-uHPLC- AB-101) = 1.47 min, (ES⁺)(M + H)⁺ 351 6

333.34 5-[(5- Methoxypyridin-2- yl)methoxy]-2- (pyridin-4-yl)-1,3-benzoxazole Tr(MET-uHPLC- AB-101) = 2.45 min, (ES⁺) (M + H)⁺ 334 7

306.32 5-[(1-Methyl-1H- pyrazol-4- yl)methoxy]-2- (pyridin-3-yl)-1,3-benzoxazole Tr(MET-uHPLC- AB-101) = 2.4 min, (ES⁺) (M + H)⁺ 307 8

403.47 Dimethyl({3-[4- ({[2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]oxy}methyl) phenoxy]propyl}) amine Tr(MET-uHPLC- AB-101) = 2.01 min,(ES⁺) (M + H)⁺ 404Method 15

Step 1, Method 15:N-Methoxy-N-methyl-2-[2-(pyridin-3-yl)-1,3-benzoxazol-6-yl]acetamide

To a stirred solution of 2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]aceticacid (200 mg, 0.79 mmol) in N,N-dimethylformamide (2 mL), was addedN-methoxymethanamine hydrochloride (92 mg, 0.94 mmol),1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium3-oxide hexafluorophosphate (329 mg, 0.86 mmol) anddiisopropylethylamine (0.41 mL, 2.36 mmol). The mixture was stirred atroom temperature for 2 hours then partitioned between ethyl acetate (20mL) and water (20 mL). The organic extract was dried over sodiumsulfate, filtered and concentrated. Purification by FCC (silica, 50-100%ethyl acetate in heptane) to give a white solid, which was dissolved inethyl acetate (20 mL) and washed with water (2×15 mL). The organicextract was dried over sodium sulfate, filtered and concentrated to givethe title compound 162 mg (69% yield) as a white solid.Tr(METCR1278)=1.54 min, (ES⁺) (M+H)⁺ 298.

Step 2, Method 15:1-(Pyridin-2-yl)-2-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]ethan-1-one

To a solution of 2-bromopyridine (94 mg, 0.59 mmol) in tetrahydrofuran(4 mL) at −78° C. was added drop-wise n-butyllithium (1.6 M solution inhexanes, 0.40 mL, 0.64 mmol). After stirring for 30 minutes at −78° C.,a solution ofN-methoxy-N-methyl-2-[2-(pyridin-3-yl)-1,3-benzoxazol-6-yl]acetamide(160 mg, 0.54 mmol) in tetrahydrofuran (2 mL) was added drop-wise. Thereaction was then stirred at −78° C. for 1 hour, then allowed to warm toroom temperature and stirred for 1 hour. The mixture was cooled to −78°C. and quenched using saturated ammonium chloride (1 mL). The mixturewas then diluted with water (30 mL) and extracted with ethyl acetate(2×30 mL). The combined organic extracts were dried over sodium sulfate,filtered and concentrated. Purification by FCC (silica, 0-100% ethylacetate in heptane) gave the title compound 44 mg (26% yield) as a whitesolid. δ_(H) NMR (500 MHz, chloroform) 9.46 (d, J=1.6 Hz, 1H), 8.79-8.73(m, 2H), 8.51 (dt, J=8.0, 1.9 Hz, 1H), 8.07 (d, J=7.8 Hz, 1H), 7.84 (td,J=7.7, 1.7 Hz, 1H), 7.78 (d, J=1.3 Hz, 1H), 7.56 (d, J=8.4 Hz, 1H),7.53-7.45 (m, 2H), 7.38 (dd, J=8.4, 1.6 Hz, 1H), 4.70 (s, 2H).Tr(MET-uHPLC-AB-101)=2.82 min, (ES⁺) (M+H)⁺316.

Step 3, Method 15:1-(Pyridin-2-yl)-2-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]ethan-1-ol

Sodium borohydride (5 mg, 0.13 mmol) was added to a stirred solution of1-(pyridin-2-yl)-2-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]ethan-1-one (34mg, 0.11 mmol) in anhydrous tetrahydrofuran (1 mL) and methanol (0.044mL, 1.08 mmol) under nitrogen at room temperature. The reaction wasstirred at this temperature for 2 hours. The mixture was quenched usingwater (0.5 mL), diluted with water (15 mL) and extracted with ethylacetate (2×15 mL). The combined organic extract were dried over sodiumsulfate, filtered and concentrated. Purification by FCC (silica, 20-100%ethyl acetate in heptane) gave the title compound 7 mg (20% yield) as awhite solid.

Example 1, Method 15:1-(Pyridin-2-yl)-2-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]ethan-1-ol

δ_(H) NMR (500 MHz, DMSO) 9.33 (s, 1H), 8.80 (d, J=4.2 Hz, 1H),8.60-8.47 (m, 2H), 7.78 (t, J=7.6 Hz, 1H), 7.70-7.62 (m, 2H), 7.59 (s,1H), 7.46 (d, J=7.8 Hz, 1H), 7.31-7.23 (m, 2H), 5.55 (br. s, 1H), 4.89(dd, J=7.6, 4.5 Hz, 1H), 3.27 (dd, J=13.8, 4.4 Hz, 1H), 3.04 (dd,J=13.6, 8.0 Hz, 1H). Tr(MET-uHPLC-AB-101)=1.43 min, (ES⁺) (M+H)⁺ 318.

The following examples were prepared using Method 15 described above:

TABLE 16 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

317.34 1-(Pyridin-2-yl)-2- [2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]ethan-1-ol Tr(MET-uHPLC- AB-101) = 1.43 min, (ES⁺) (M + H)⁺ 318 2

315.33 1-(Pyridin-2-yl)-2- [2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]ethan-1-one Tr(MET-uHPLC- AB-101) = 2.82 min, (ES⁺) (M + H)⁺ 316Method 16

Step 1, Method 16:6-Methoxy-2-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]-1,2-dihydroisoquinolin-1-one

6-Methoxyisoquinolin-1(2H)-one (64 mg, 0.36 mmol),5-bromo-2-(pyridin-3-yl)-1,3-benzoxazole (150 mg, 0.55 mmol), copper(I)iodide (14 mg, 0.07 mmol), L-proline (17 mg, 0.15 mmol) and anhydrouspotassium carbonate (100 mg, 0.73 mmol) were placed in a round bottomflask under nitrogen. DMSO (5 mL) was added and the mixture heated to120° C. overnight. Water (6 mL) and ethyl acetate (10 mL) were added andthe mixture filtered. The solid was washed with ethyl acetate (2×5 mL)and water (2×2 mL) and recrystallised from a mixture of methanol (40 mL)and DMSO (3 mL) with hot filtration to give the title compound 23 mg(17% yield) as an off white powder.

Example 1, Method 16:6-Methoxy-2-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]-1,2-dihydroisoquinolin-1-one

δ_(H) NMR (500 MHz, DMSO) 9.41 (br. s, 1H), 8.85 (br. s, 1H), 8.59 (d,J=8.0 Hz, 1H), 8.18 (d, J=8.8 Hz, 1H), 8.00-7.94 (m, 2H), 7.69 (dd,J=7.9, 4.8 Hz, 1H), 7.55 (dd, J=8.6, 2.1 Hz, 1H), 7.51 (d, J=7.4 Hz,1H), 7.23 (d, J=2.5 Hz, 1H), 7.14 (dd, J=8.9, 2.5 Hz, 1H), 6.69 (d,J=7.4 Hz, 1H), 3.91 (s, 3H). Tr(MET-uHPLC-AB-101)=2.86 min, (ES⁺) (M+H)⁺370.

The following example was prepared using Method 16 described above:

TABLE 17 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

369.37 6-Methoxy-2-[2- (pyridin-3-yl)-1,3- benzoxazol- 5-yl]1,2-dihydroisoquinolin- 1-one Tr(MET-uHPLC- AB-101) = 2.86 min, (ES⁺) (M +H)⁺ 370Method 17

Step 1, Method 17:2-(Pyridin-3-yl)-N-[2,2,2-trifluoro-1-(4-methoxyphenyl)ethyl]-[1,3]oxazolo[5,4-b]pyridin-6-amine

To a stirred solution of 2,2,2-trifluoro-1-(4-methoxyphenyl)ethanone (51mg, 0.25 mmol) in tetrahydrofuran (2.5 mL) at −78° C., was added 1 Mtitanium(IV) chloride in dichloromethane (0.25 mL, 0.25 mmol). Themixture was then left stirring for 10 minutes at −78° C., then2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-amine (53 mg, 0.25 mmol,prepared by Method 19) was added and the mixture was allowed to warm toroom temperature. Triethyamine (0.1 mL, 0.75 mmol) was added and themixture stirred at room temperature for 3 hours. Methanol (0.2 mL)followed by sodium borohydride (28 mg, 0.75 mmol) were added to themixture and the mixture was stirred at room temperature overnight. Themixture was treated with sodium borohydride (28 mg, 0.75 mmol) andstirred at room temperature overnight. The mixture was diluted withwater (15 mL) and extracted with ethyl acetate (2×15 mL). The combinedorganic extracts were dried over sodium sulfate, filtered andconcentrated. Purification by preparative HPLC (acetonitrile/water) gavethe title compound 1.7 mg (yield 2%) as a brown solid.

Example 1, Method 17:2-(Pyridin-3-yl)-N-[2,2,2-trifluoro-1-(4-methoxyphenyl)ethyl]-[1,3]oxazolo[5,4-b]pyridin-6-amine

δ_(H) NMR (500 MHz, DMSO) 9.29 (d, J=1.7 Hz, 1H), 8.80 (dd, J=4.8, 1.6Hz, 1H), 8.48 (dt, J=8.0, 1.9 Hz, 1H), 8.06 (d, J=2.6 Hz, 1H), 7.66 (d,J=2.6 Hz, 1H), 7.64 (dd, J=8.0, 4.9 Hz, 1H), 7.56 (d, J=8.7 Hz, 2H),7.08 (d, J=10.3 Hz, 1H), 6.97 (d, J=8.8 Hz, 2H), 5.64 (p, J=8.4, 7.9 Hz,1H), 3.74 (s, 3H). Tr(MET-uHPLC-AB-101)=3.23 min, (ES⁺) (M+H)⁺ 401.

The following example was prepared using Method 17 described above:

TABLE 18 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

400.35 2-(Pyridin-3-yl)-N- [2,2,2-trifluoro-1-(4- methoxyphenyl)ethyl]-[1,3]oxazolo[5,4- b]pyridin-6-amine Tr(MET-uHPLC- AB-101) = 3.23 min,(ES⁺) (M + H)⁺ 401Method 18

Step 1, Method 18:3-{6-[2-(4-Methoxyphenyl)ethynyl]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine

A mixture of 3-{6-bromo-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine (50 mg,0.18 mmol, prepared by Method 11), 1-ethynyl-4-methoxybenzene (72 mg,0.54 mmol) and copper(I) iodide (3 mg, 0.013 mmol) in 1,4-dioxane (1.5mL) and triethylamine (0.13 mL, 0.90 mmol) was degassed under a streamof nitrogen for 10 minutes. Palladium(II) chloride-triphenylphosphine(1:2:2) (9 mg, 0.013 mmol) was added and the mixture was stirred at 80°C. for 2 hours. The reaction was then scaled-up following the sameprocedure with 3-{6-bromo-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine (200mg, 0.72 mmol), 1-ethynyl-4-methoxybenzene (287 mg, 2.17 mmol),copper(I) iodide (10 mg, 0.053 mmol), triethylamine (0.50 mL, 3.61 mmol)and palladium(II) chloride-triphenylphosphine (1:2:2) (37 mg, 0.052mmol) in 1,4-dioxane (6 mL) and stirred at 80° C. for 2.5 hours. Bothreaction mixtures were then combined, diluted with water (35 mL) andextracted with ethyl acetate (2×35 mL). The combined organic extractswere dried over sodium sulfate, filtered and concentrated. Purificationby FCC (silica, 0-100% ethyl acetate in heptane followed by 0-10%methanol in dichloromethane) gave the title compound 188 mg (63% yield)as a brown solid. Tr(METCR1278)=2.24 min, (ES⁺) (M+H)⁺ 328.

Step 2, Method 18:3-{6-[(Z)-2-(4-Methoxyphenyl)ethenyl]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine

To a stirred solution of3-{6-[2-(4-methoxyphenyl)ethynyl]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine(88 mg, 0.27 mmol) and quinoline (0.032 mL, 0.27 mmol) intetrahydrofuran (4 mL) and ethanol (4 mL) under nitrogen in a pressurevessel, was added Lindlar's catalyst (9 mg, 0.032 mmol). The mixture wasplaced under a hydrogen atmosphere (1 bar), heated to 80° C. and stirredat this temperature overnight. The mixture was filtered and rinsed withtetrahydrofuran (10 mL) then the filtrate was concentrated. The mixturewas then treated with Lindlar's catalyst (8.6 mg, 0.032 mmol), placedunder a hydrogen atmosphere (3.5 bars), heated to 80° C. and stirred atthis temperature overnight. The mixture was filtered and rinsed withtetrahydrofuran (10 mL). The filtrate was concentrated and purified byFCC (silica, 0-3% methanol in dichloromethane) and preparative HPLC(acetonitrile/water) to give the title compound 6.2 mg (7% yield) as awhite powder.

Example 1, Method 18:3-{6-[(Z)-2-(4-Methoxyphenyl)ethenyl]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine

δ_(H) NMR (500 MHz, DMSO) 9.35 (d, J=1.9 Hz, 1H), 8.84 (dd, J=4.8, 1.6Hz, 1H), 8.54 (dt, J=8.0, 1.9 Hz, 1H), 8.25 (d, J=1.8 Hz, 1H), 8.05 (d,J=1.8 Hz, 1H), 7.67 (dd, J=8.0, 4.8 Hz, 1H), 7.17 (d, J=8.7 Hz, 2H),6.85 (d, J=8.7 Hz, 2H), 6.79 (d, J=12.1 Hz, 1H), 6.69 (d, J 12.1 Hz,1H), 3.74 (s, 3H). Tr(MET-uHPLC-AB-101)=3.53 min, (ES⁺) (M+H)⁺ 330.

The following examples were prepared using Method 18 described above:

TABLE 19 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

329.35 3-{6-[2-(4- Methoxyphenyl)ethenyl]- [1,3]oxazolo[5,4-b]pyridin-2- yl}pyridine Tr(MET-uHPLC- AB-101) = 3.53 min, (ES⁺) (M +H)⁺ 330 2

327.34 3-{6-[(Z)-2-(4- Methoxyphenyl)ethenyl]- [1,3]oxazolo[5,4-b]pyridin-2- yl}pyridine Tr(MET-uHPLC- AB-101) = 3.73 min, (ES⁺) (M +H)⁺ 328 3

298.30 3-{6-[2-(Pyridin-3- yl)ethynyl]- [1,3]oxazolo[5,4- b]pyridin-2-yl}pyridine Tr(MET-uHPLC- AB-101) = 2.55 min, (ES⁺) (M + H)⁺ 299Method 19

Step 1, Method 19: 2-(Pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-amine

A pressure tube was charged with9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphane (189 mg, 0.33mmol), tris(dibenzylideneacetone)dipalladium(0) (100 mg, 0.11 mmol),3-{6-bromo-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine (300 mg, 1.09 mmol,prepared by Method 11), diphenylmethanimine (236 mg, 1.30 mmol) andcaesium carbonate (1.06 g, 3.26 mmol) in N,N-dimethylacetamide (6 mL).The mixture was degassed using a flow of nitrogen for 10 minutes. Themixture was then heated to 110° C. and stirred at this temperatureovernight. The mixture was then diluted with water (70 mL) and extractedwith ethyl acetate (2×70 mL). The combined organic extracts were driedover sodium sulfate, filtered and concentrated. The residue was dilutedwith tetrahydrofuran (15 mL), 2 M hydrochloric acid was added (6 mL) andthe mixture was left standing at room temperature for 1 hour. Themixture was diluted with water (30 mL) and extracted with ethyl acetate(30 mL). The aqueous extract was then basified using saturated sodiumbicarbonate solution to pH 8-9 and extracted with ethyl acetate (2×50mL). The organic extracts were dried over sodium sulfate, filtered andconcentrated. The solid was triturated with dichloromethane to give thetitle compound 94 mg as a light brown solid. The filtrate wasconcentrated then purified by FCC (silica, 0-100% heptane in ethylacetate followed by 10% methanol in dichloromethane) to give the titlecompound 18 mg (total 112 mg, 40% yield) as a light brown solid.Tr(METCR1278)=1.17 min, (ES⁺) (M+H)⁺ 213.

Step 2, Method 19:5-Methoxy-2-[2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]-2,3-dihydro-1H-isoindol-1-one

To sodium hydride (60% in mineral oil, 15 mg, 0.37 mmol) under nitrogenwas added a solution of2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-amine (50 mg, 0.18 mmol)in tetrahydrofuran (2 mL). The suspension was stirred at roomtemperature for 10 minutes. Ethyl 2-(bromomethyl)-4-methoxybenzoate (50mg, 0.18 mmol, described in WO2009042907) in tetrahydrofuran (1 mL) wasadded and the mixture stirred at room temperature for 1 hour. Themixture was heated to 60° C. and stirred for 2 hours, then stood at roomtemperature overnight. The mixture was diluted with water (6 mL) andfiltered to give a brown solid (22 mg). Recrystallization from DMSO (1mL) and acetonitrile (1 mL) and recrystallisation from DMSO (2 mL) gavethe title compound 1.5 mg (2% yield) as an off-white powder.

Example 1, Method 19:5-Methoxy-2-[2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]-2,3-dihydro-1H-isoindol-1-one

δ_(H) NMR (250 MHz, DMSO) 9.40 (s, 1H), 8.90 (d, J=2.4 Hz, 1H), 8.85 (d,J=5.5 Hz, 1H), 8.74 (d, J=2.4 Hz, 1H), 8.57 (dt, J=8.0, 1.9 Hz, 1H),7.76 (d, J=8.5 Hz, 1H), 7.67 (dd, J=8.3, 4.6 Hz, 1H), 7.28-7.20 (m, 1H),7.13 (dd, J=8.4, 2.2 Hz, 1H), 5.10 (s, 2H), 3.93 (s, 3H).Tr(MET-uHPLC-AB-101)=2.67 min, (ES⁺) (M+H)⁺ 359.

The following example was prepared using Method 19 described above:

TABLE 20 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

358.35 5-Methoxy-2-[2- (pyridin-3-yl)-[1,3]- b]oxazolo[5,4-b]pyridin-6-yl]- 2,3-dihydro-1H- isoindol-1-one Tr(MET-uHPLC- AB-101) =2.67 min, (ES⁺) (M + H)⁺ 359Method 20

Step 1, Method 20: Methyl 5-methoxypyrazine-2-carboxylate

To methyl 5-chloropyrazine-2-carboxylate (2.00 g, 11.6 mmol) undernitrogen, was added a 0.5 M solution of sodium methoxide in methanol(27.8 mL, 13.9 mmol). The mixture was refluxed at 90° C. for 15 minutes.Water (80 mL) was added and the mixture extracted with ethyl acetate(2×100 mL). The combined organic extracts were dried over sodiumsulfate, filtered and concentrated to give the title compound 1.68 g(79% yield) as a white powder. δ_(H) NMR (500 MHz, chloroform) 8.88 (d,J=1.2 Hz, 1H), 8.28 (d, J=1.2 Hz, 1H), 4.05 (s, 3H), 4.00 (s, 3H).Tr(METCR1278)=1.23 min, (ES⁺) (M+H)⁺ 169.

Step 2, Method 20: (5-Methoxypyrazin-2-yl)methanol

Sodium borohydride (270 mg, 7.14 mmol) was added to a stirred solutionof methyl 5-methoxypyrazine-2-carboxylate (200 mg, 1.19 mmol) inanhydrous tetrahydrofuran (8 mL) under nitrogen. The mixture wasrefluxed at 65° C. for 15 minutes, after which methanol (1.59 mL, 39.2mmol) was added slowly. The reaction was refluxed at 65° C. for 1.5hours. The mixture was quenched with water (0.5 mL), then diluted withwater (15 mL), extracted with ethyl acetate (2×25 mL) then 20%2-propanol in dichloromethane (25 mL). The combined organic extractswere dried over sodium sulfate, filtered and concentrated to give thetitle compound 115 mg (69% yield) as a white crystalline solid. δ_(H)NMR (500 MHz, DMSO) 8.28-8.16 (m, 2H), 5.41 (t, J=5.8 Hz, 1H), 4.54 (d,J=5.6 Hz, 2H), 3.90 (s, 3H). Tr(METCR1278)=0.74 min, (ES⁺) (M+H)⁺ 141.

Step 3, Method 20: (5-Methoxypyrazin-2-yl)methyl methanesulfonate

To a stirred solution of (5-methoxypyrazin-2-yl)methanol (73 mg, 0.52mmol) in dichloromethane (1 mL) under nitrogen, was added triethylamine(0.08 mL, 0.73 mmol) followed by methanesulfonyl chloride (0.042 mL,0.55 mmol). The mixture was stirred at room temperature for 1 hour. Themixture was then partitioned between dichloromethane (10 mL) and water(10 mL). The organic extract was dried over sodium sulfate, filtered andconcentrated to give the title compound 59 mg (52% yield) as a yellowoil. Tr(METCR1278)=1.25 min, (ES⁺) (M+H)⁺ 219.

Step 4, Method 20:5-[(5-Methoxypyrazin-2-yl)methoxy]-2-(pyridin-3-yl)-1,3-benzoxazole

To sodium hydride (60% in mineral oil, 11.8 mg, 0.29 mmol) undernitrogen, was added a solution of 2-(pyridin-3-yl)-1,3-benzoxazol-5-ol(57 mg, 0.27 mmol, prepared by Method 14) in N,N-dimethylformamide (1mL) and the mixture was stirred at room temperature for 30 minutes. Asolution of (5-methoxypyrazin-2-yl)methyl methanesulfonate (59 mg, 0.27mmol) in N,N-dimethylformamide (0.5 mL) was added and the mixture wasstirred at room temperature overnight. The mixture was quenched withwater (2 mL) and filtered to give a solid, which was purified by FCC(silica, 0-3% methanol in dichloromethane) to give the title compound20.8 mg (23% yield) as an off-white powder.

Example 1, Method 20:5-[(5-Methoxypyrazin-2-yl)methoxy]-2-(pyridin-3-yl)-1,3-benzoxazole

δ_(H) NMR (500 MHz, DMSO) 9.32 (s, 1H), 8.86-8.75 (m, 1H), 8.56-8.47 (m,1H), 8.42 (s, 1H), 8.35 (s, 1H), 7.74 (d, J=8.9 Hz, 1H), 7.68-7.61 (m,1H), 7.54 (s, 1H), 7.14 (d, J=8.9 Hz, 1H), 5.23 (s, 2H), 3.92 (s, 3H).Tr(MET-uHPLC-AB-101)=2.94 min, (ES⁺) (M+H)⁺ 335.

The following example was prepared using Method 20 described above:

TABLE 21 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

334.33 5-[(5- methoxypyrazin-2- yl)methoxy]-2- (pyridin-3-yl)-1,3-benzoxazole Tr(MET-uHPLC- AB-101) = 2.94 min, (ES⁺) (M + H)⁺ 335Method 21

Step 1, Method 21:3-Methoxy-6-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]-5H,6H,7H-pyrrolo[3,4-b]pyridin-7-one

To sodium hydride (60% in mineral oil, 15 mg, 0.38 mmol) and2-(pyridin-3-yl)-1,3-benzoxazol-5-amine (41 mg, 0.19 mmol) undernitrogen was added tetrahydrofuran (2 mL). The suspension was stirred atroom temperature for 10 minutes. Methyl3-(bromomethyl)-5-methoxypyridine-2-carboxylate (50 mg, 0.19 mmol,described in Heterocycles (2013), 87(10), 2071-2079) in tetrahydrofuran(1 mL) was then added and the mixture was stirred at 60° C. for 2 hours,then at 70° C. for 2 hours, then at 80° C. for 2 hours, followed bystirring at room temperature for 2 days. The mixture was diluted withwater (2 mL) and filtered to give a solid, which was triturated in ethylacetate (2 mL) to give the title compound 18 mg (26% yield) as a brownpowder.

Example 1, Method 21:3-Methoxy-6-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]-5H,6H,7H-pyrrolo[3,4-b]pyridin-7-one

δ_(H) NMR (250 MHz, DMSO) 9.38 (d, J=1.5 Hz, 1H), 8.81 (dd, J=4.8, 1.7Hz, 1H), 8.54 (dt, J=8.0, 2.1 Hz, 1H), 8.48 (d, J=2.7 Hz, 1H), 8.31 (d,J=1.9 Hz, 1H), 8.02 (dd, J=8.9, 2.2 Hz, 1H), 7.86 (d, J=9.0 Hz, 1H),7.73-7.58 (m, 2H), 5.06 (s, 2H), 3.99 (s, 3H). Tr(MET-uHPLC-AB-101)=2.26min, (ES⁺) (M+H)⁺ 359.

The following example was prepared using Method 21 described above:

TABLE 22 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

358.35 3-Methoxy-6-[2- (pyridin-3-yl)-1,3- benzoxazol-5-yl] 5H,6H,7H-pyrrolo[3,4- b]pyridin-7-one Tr(MET-uHPLC- AB-101) = 2.26 min, (ES⁺)(M + H)⁺ 359Method 22

Step 1, Method 22: N-(2,4-Dihydroxyphenyl)pyridine-3-carboxamide

To a stirred solution of 4-aminobenzene-1,3-diol hydrochloride (0.50 g,3.09 mmol) in pyridine (6 mL) with ice cooling, was added nicotinoylchloride hydrochloride (0.55 g, 3.09 mmol) portion-wise. The mixture wasstirred at room temperature for 16 hours. The mixture was concentratedin vacuo and the residue was diluted with water (50 mL) and extractedwith ethyl acetate (2×60 mL). The combined organic extracts were driedover sodium sulfate, filtered and concentrated. Purification by FCC(silica, 30-100% ethyl acetate in heptane) gave the title compound 148mg (21% yield) as a light brown solid. δ_(H) NMR (250 MHz, DMSO) 9.47(d, J=88.0 Hz, 3H), 9.10 (d, J=1.7 Hz, 1H), 8.73 (dd, J=4.8, 1.5 Hz,1H), 8.28 (dt, J=7.9, 1.9 Hz, 1H), 7.53 (dd, J=7.7, 5.1 Hz, 1H), 7.20(d, J=8.6 Hz, 1H), 6.36 (d, J=2.6 Hz, 1H), 6.24 (dd, J=8.6, 2.6 Hz, 1H).Tr(METCR1278)=0.79 min, (ES⁺) (M+H)⁺ 231.

Step 2, Method 22: 2-(Pyridin-3-yl)-1,3-benzoxazol-6-ol

N-(2,4-dihydroxyphenyl)pyridine-3-carboxamide (150 mg, 0.65 mmol) andacetic acid (3 mL) were heated at 200° C. for 30 minutes in a microwave.The mixture was then concentrated in vacuo and the residue wastriturated in ethyl acetate (10 mL) to give the title compound 55 mg(40% yield) as a light brown powder. δ_(H) NMR (500 MHz, DMSO) 9.96 (s,1H), 9.28 (d, J=1.7 Hz, 1H), 8.76 (dd, J=4.8, 1.5 Hz, 1H), 8.45 (dt,J=8.0, 1.9 Hz, 1H), 7.67-7.59 (m, 2H), 7.12 (d, J=2.2 Hz, 1H), 6.89 (dd,J=8.6, 2.3 Hz, 1H). Tr(METCR1278)=1.38 min, (ES⁺) (M+H)⁺ 213.

Step 3, Method 22:2-(Pyridin-3-yl)-6-(pyridin-3-ylmethoxy)-1,3-benzoxazole

To sodium hydride (60% in mineral oil, 10 mg, 0.25 mmol) under nitrogen,was added a solution of 2-(pyridin-3-yl)-1,3-benzoxazol-6-ol (50 mg,0.24 mmol) in N,N-dimethylformamide (1 mL) and the mixture was stirredat room temperature for 30 minutes. Sodium hydride (60% in mineral oil,10 mg, 0.25 mmol) and 3-(bromomethyl)pyridine hydrobromide (66 mg, 0.26mmol) were dissolved in N,N-dimethylformamide (1 mL) and stirred at roomtemperature for 10 minutes. This suspension was then added to reactionmixture and the mixture was stirred at room temperature for 1 hour. Themixture was quenched with water (0.5 mL), then diluted with water (15mL) and extracted with ethyl acetate (2×15 mL). The combined organicextracts were dried over sodium sulfate, filtered and concentrated.Purification by FCC (silica, 0 to 3% methanol in dichloromethane) gavethe title compound 39 mg (55% yield) as an off-white powder.

Example 1, Method 22:2-(Pyridin-3-yl)-6-(pyridin-3-ylmethoxy)-1,3-benzoxazole

δ_(H) NMR (500 MHz, DMSO) 9.30 (d, J=1.8 Hz, 1H), 8.78 (dd, J=4.8, 1.6Hz, 1H), 8.72 (d, J=1.9 Hz, 1H), 8.57 (dd, J=4.8, 1.6 Hz, 1H), 8.48 (dt,J=8.0, 1.9 Hz, 1H), 7.92 (dt, J=7.8, 1.9 Hz, 1H), 7.76 (d, J=8.7 Hz,1H), 7.64 (dd, J=8.0, 4.8 Hz, 1H), 7.58 (d, J=2.4 Hz, 1H), 7.45 (dd,J=7.8, 4.8 Hz, 1H), 7.14 (dd, J=8.7, 2.4 Hz, 1H), 5.27 (s, 2H).Tr(MET-uHPLC-AB-101)=1.68 min, (ES⁺) (M+H)⁺ 304.

The following example was prepared using Method 22 described above:

TABLE 23 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

303.31 2-(Pyridin-3-yl)-6- (pyridin-3- ylmethoxy)-1,3- benzoxazoleTr(MET-uHPLC- AB-101) = 1.68 min, (ES⁺) (M + H)⁺ 304Method 23

Step 1, Method 23: Methyl 2-(pyridin-3-yl)-1,3-benzoxazole-5-carboxylate

Methyl 3-amino-4-hydroxybenzoate (200 mg, 1.2 mmol) was suspended in1,4-dioxane (3 mL) and pyridine-3-carbonyl chloride hydrochloride (234mg, 1.32 mmol) was added and the mixture heated to 200° C. for 15 min ina microwave. This procedure was performed 5 times. All reaction mixtureswere combined then partitioned between ethyl acetate (100 mL) andsaturated aqueous sodium bicarbonate (80 mL). The organic extract wasdried over sodium sulfate, filtered and concentrated. Purification byFCC (silica, 20-100% ethyl acetate in heptane) gave the title compound560 mg (37% yield) as a light brown solid. δ_(H) NMR (500 MHz, DMSO)9.37 (d, J=1.7 Hz, 1H), 8.84 (dd, J=4.8, 1.6 Hz, 1H), 8.56 (dt, J=8.0,1.9 Hz, 1H), 8.37 (d, J=1.4 Hz, 1H), 8.09 (dd, J=8.6, 1.7 Hz, 1H), 7.97(d, J=8.6 Hz, 1H), 7.68 (ddd, J=8.0, 4.8, 0.7 Hz, 1H), 3.91 (s, 3H).Tr(METCR1278)=1.74 min, (ES⁺) (M+H)⁺ 255.

Step 2, Method 23: [2-(Pyridin-3-yl)-1,3-benzoxazol-5-yl]methanol

4 M lithium aluminum hydride in tetrahydrofuran (0.25 mL, 1.00 mmol) wasadded to a stirred solution of methyl2-(pyridin-3-yl)-1,3-benzoxazole-5-carboxylate (340 mg, 1.34 mmol) inanhydrous tetrahydrofuran (12 mL) under nitrogen. The mixture wasstirred at 0° C. for 30 minutes. The mixture was quenched by cautiousaddition of water (1 mL) followed by saturated ammonium chloridesolution (0.5 mL). The mixture was stirred at 0° C. for 20 minutes. Themixture was diluted with water (15 mL) and extracted with ethyl acetate(2×15 mL). The organic extracts were dried over sodium sulfate, filteredand concentrated. Purification by FCC (silica, 0-15% methanol indichloromethane) gave the title compound 197 mg (65% yield) as anoff-white solid. Tr(MET-uHPLC-AB-101)=1.7 min, (ES⁺) (M+H)⁺ 227.

Step 3, Method 23: 5-(Chloromethyl)-2-(pyridin-3-yl)-1,3-benzoxazole

To a stirred solution of [2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]methanol(50 mg, 0.22 mmol) in dichloromethane (1 mL) under nitrogen with icecooling, was added triethylamine (0.068 mL, 0.48 mmol) followed bymethansulfonyl chloride (0.036 mL, 0.46 mmol). The mixture was thenallowed to warm to room temperature and stirred for 48 hours. Themixture was retreated with triethylamine (0.068 mL, 0.48 mmol) andmethanesulfonyl chloride (0.036 mL, 0.46 mmol) and stirred at roomtemperature for 2 hours. The mixture was partitioned betweendichloromethane (10 mL) and water (10 mL). The organic extract was driedover sodium sulfate, filtered and concentrated to give the titlecompound 75 mg (91% yield) as an orange solid. Tr(METCR1278)=1.86 min,(ES⁺) (M+H)⁺ 245.

Step 4, Method 23:5-{[(5-Methoxypyridin-2-yl)oxy]methyl}-2-(pyridin-3-yl)-1,3-benzoxazole

A suspension of 5-(chloromethyl)-2-(pyridin-3-yl)-1,3-benzoxazole (50mg, 0.20 mmol), 5-methoxy-1,2-dihydropyridin-2-one (28 mg, 0.22 mmol)and silver carbonate (38 mg, 0.14 mmol) in toluene (2 mL) was stirred at80° C. for 24 hours. The mixture was diluted with water (20 mL) andextracted with ethyl acetate (2×20 mL). The combined organic extractswere dried over sodium sulfate, filtered and concentrated. Purificationby preparative HPLC (acetonitrile/water) gave the title compound 2.4 mg(4% yield) as an off-white powder.

Example 1, Method 23:54[(5-Methoxypyridin-2-yl)oxy]methyl)-2-(pyridin-3-yl)-1,3-benzoxazole

δ_(H) NMR (500 MHz, DMSO) 9.35 (d, J=2.0 Hz, 1H), 8.81 (dd, J=4.8, 1.5Hz, 1H), 8.54 (dt, J=8.0, 1.9 Hz, 1H), 7.91 (s, 1H), 7.87 (d, J=3.1 Hz,1H), 7.82 (d, J=8.4 Hz, 1H), 7.66 (dd, J=8.0, 4.8 Hz, 1H), 7.55 (dd,J=8.4, 1.5 Hz, 1H), 7.42 (dd, J=8.9, 3.1 Hz, 1H), 6.87 (d, J=8.9 Hz,1H), 5.42 (s, 2H), 3.77 (s, 3H). Tr(MET-uHPLC-AB-101)=3.22 min, (ES⁺)(M+H)⁺ 334.

The following examples were prepared using Method 23 described above:

TABLE 24 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

333.34 5-{[(5- Methoxypyridin-2- yl)oxy]methyl}-2- (pyridin-3-yl)-1,3-benzoxazole Tr(MET-uHPLC- AB-101) = 3.22 min, (ES⁺) (M + H)⁺ 334Method 24

Step 1, Method 24: 5-(Chloromethyl)pyrimidine hydrochloride

To a solution of pyrimidin-5-ylmethanol (48 mg, 0.43 mmol) indichloromethane (3 mL), thionyl dichloride (0.26 mL, 3.6 mmol) was addeddropwise slowly at 0° C. The mixture was heated to reflux (50° C.) for 2hours and then the mixture was concentrated. Dichloromethane (5 mL) wasadded and the mixture was concentrated (×3) to give the title compoundas a yellow oil which was used directly in the next step.Tr(METCR1278)=0.90 min, (ES⁺) (M+H)⁺ 129/131.

Step 2, Method 24:4-[5-(Pyrimidin-5-ylmethoxy)-1-benzofuran-2-yl]pyridine-3-carbonitrile

4-(5-Hydroxy-1-benzofuran-2-yl)pyridine-3-carbonitrile (90%, 80 mg, 0.3mmol, prepared by Method 9), 5-(chloromethyl)pyrimidine hydrochloride(0.43 mmol) and potassium iodide (56 mg, 0.34 mmol) were dissolved inanhydrous N,N-dimethylformamide (6 mL) and stirred for 5 minutes at roomtemperature. Sodium hydride (60% in mineral oil, 37 mg, 0.91 mmol) wasadded and the reaction mixture was stirred at room temperature for 3hours. Water (0.1 mL) was added and the solvents were removed in vacuo.The residue was partitioned between ethyl acetate (50 mL) and water (50mL) and the aqueous was extracted with ethyl acetate (2×50 mL). Thecombined organic extracts were washed with water (20 mL), brine (20 mL),dried over sodium sulfate, filtered and concentrated. Purification byFCC (silica, 0-80% ethyl acetate in heptane) gave the title compound30.3 mg (30% yield) as an off-white solid.

Example 1, Method 24:4-[5-(Pyrimidin-5-ylmethoxy)-1-benzofuran-2-yl]pyridine-3-carbonitrile

δ_(H) NMR (500 MHz, DMSO) 9.19 (s, 1H), 9.12 (s, 1H), 8.96 (s, 2H), 8.92(d, J=5.4 Hz, 1H), 8.08 (d, J=5.5 Hz, 1H), 7.96 (s, 1H), 7.67 (d, J=9.0Hz, 1H), 7.53 (d, J=2.6 Hz, 1H), 7.21 (dd, J=9.0, 2.6 Hz, 1H), 5.26 (s,2H). Tr(MET-uHPLC-AB-101)=2.8 min, (ES⁺) (M+H)⁺ 329.

The following example was prepared using Method 24 described above:

TABLE 25 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

328.32 4-[5-(Pyrimidin-5- ylmethoxy)-1- benzofuran-2- yl]pyridine-3-carbonitrile Tr(MET-uHPLC- AB-101) = 2.8 min, (ES⁺) (M + H)⁺ 329Method 25

Step 1, Method 25: 1-(5-Methoxypyridin-2-yl)ethan-1-ol

To a stirred solution of 5-methoxypyridine-2-carbaldehyde (220 mg, 1.60mmol) in tetrahydrofuran (3 mL) with ice cooling was added 1.4 M methylmagnesium bromide in tetrahydrofuran (1.15 mL, 1.60 mmol). The mixturewas stirred for 30 minutes with ice cooling. The mixture was quenchedwith saturated aqueous ammonium chloride solution (0.5 mL), diluted withwater (15 mL) and extracted with ethyl acetate (2×15 mL). The combinedorganic extracts were dried over sodium sulfate, filtered andconcentrated to give the title compound 218 mg (89% yield) as a yellowoil. 8H NMR (500 MHz, DMSO) 8.17 (d, J=2.9 Hz, 1H), 7.42 (d, J=8.6 Hz,1H), 7.36 (dd, J=8.7, 2.9 Hz, 1H), 5.23 (d, J=4.6 Hz, 1H), 4.72-4.64 (m,1H), 3.80 (s, 3H), 1.32 (d, J=6.5 Hz, 3H).

Step 2, Method 25:3-{6-[1-(5-Methoxypyridin-2-yl)ethoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine

To a stirred solution of 1-(5-methoxypyridin-2-yl)ethan-1-ol (20 mg,0.13 mmol), 2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-ol (22 mg,0.10 mmol, prepared by Method 30) and triphenylphosphine (41 mg, 0.16mmol) in anhydrous tetrahydrofuran (1 mL) at 0° C. was added diisopropylazodicarboxylate (0.031 mL, 0.16 mmol). The mixture was allowed to warmto room temperature and stirred overnight. The mixture was diluted withwater (15 mL) and extracted with ethyl acetate (2×15 mL). The combinedorganic extracts were dried over magnesium sulfate, filtered andconcentrated. Purification by FCC (silica, 50-100% ethyl acetate inheptane) and preparative HPLC (acetonitrile/water) gave the titlecompound 7.4 mg (21% yield) as a colourless, crystalline solid.

Example 2, Method 25:3{6-[1-(5-Methoxypyridin-2-yl)ethoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine

δ_(H) NMR (500 MHz, DMSO) 9.31 (d, J=1.9 Hz, 1H), 8.81 (dd, J=4.8, 1.6Hz, 1H), 8.50 (dt, J=8.0, 1.9 Hz, 1H), 8.28 (d, J=2.9 Hz, 1H), 8.12 (d,J=2.7 Hz, 1H), 7.87 (d, J=2.7 Hz, 1H), 7.65 (dd, J=7.9, 4.8 Hz, 1H),7.49 (d, J=8.7 Hz, 1H), 7.38 (dd, J=8.7, 3.0 Hz, 1H), 5.63 (q, J=6.4 Hz,1H), 3.80 (s, 3H), 1.64 (d, J=6.4 Hz, 3H). Tr(MET-uHPLC-AB-101)=2.6 min,(ES⁺) (M+H)⁺ 349.

The following example was prepared using Method 25 described above:

TABLE 26 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

348.36 3-{6-[1-(5- Methoxypyridin-2- yl)ethoxy]- [1,3]oxazolo[5,4-b]pyridin-2- yl}pyridine Tr(MET-uHPLC- AB-101) = 2.6 min, (ES⁺) (M + H)⁺349Method 26

Step 1, Method 26:4-{5-[(5-Methoxypyrazin-2-yl)methoxy]-1-benzofuran-2-yl}pyridine-3-carbonitrile

To sodium hydride (60% in mineral oil, 11.8 mg, 0.29 mmol) undernitrogen, was added a solution of4-(5-hydroxy-1-benzofuran-2-yl)pyridine-3-carbonitrile (57 mg, 0.27mmol, prepared by Method 9) in N,N-dimethylformamide (1 mL) and themixture was stirred at room temperature for 30 minutes. A solution of(5-methoxypyrazin-2-yl)methyl methanesulfonate (64 mg, 0.3 mmol,prepared by Method 20) in N,N-dimethylformamide (0.5 mL) was added andthe mixture was stirred at room temperature overnight. The mixture wasthen quenched with water (3 mL) and allowed to cool to room temperature.The resulting suspension was filtered, washed with water (3 mL),methanol (2 mL) and heptane (5 mL) to give the title compound 63 mg (65%yield) as a tan powder.

Example 1, Method 26:4-{5-[(5-Methoxypyrazin-2-yl)methoxy]-1-benzofuran-2-yl}pyridine-3-carbonitrile

δ_(H) NMR (500 MHz, DMSO) 9.12 (s, 1H), 8.92 (d, J=5.4 Hz, 1H), 8.42 (d,J=1.0 Hz, 1H), 8.35 (d, J=1.3 Hz, 1H), 8.08 (d, J=5.4 Hz, 1H), 7.95 (s,1H), 7.66 (d, J=9.0 Hz, 1H), 7.52 (d, J=2.6 Hz, 1H), 7.19 (dd, J=9.0,2.6 Hz, 1H), 5.22 (s, 2H), 3.93 (s, 3H). Tr(MET-uHPLC-AB-101)=3.5 min,(ES⁺) (M+H)⁺ 359.

The following example was prepared using Method 26 described above:

TABLE 27 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

358.35 4-{5-[(5- Methoxypyrazin-2- yl)methoxy]-1- benzofuran-2-yl}pyridine-3- carbonitrile Tr(MET-uHPLC- AB-101) = 3.5 min, (ES⁺) (M +H)⁺ 359Method 27

Step 1, Method 27: Methyl 5-(methoxymethoxy)pyridine-2-carboxylate

Sodium hydride (60% in mineral oil, 144 mg, 3.59 mmol) was suspended inanhydrous N,N-dimethylformamide (5 mL) and cooled to 0° C. Methyl5-hydroxypyridine-2-carboxylate (500 mg, 3.27 mmol) dissolved inN,N-dimethylformamide (5 mL) was added slowly to the suspension. Thereaction mixture was stirred under nitrogen and warmed to roomtemperature over 30 minutes. The reaction was cooled to 0° C. andchloro(methoxy)methane (0.26 mL, 3.43 mmol) was added drop-wise over 15minutes. The reaction was warmed to room temperature and stirred for 16hours. Water (20 mL) was added and the solvents were removed in vacuo.The mixture was partitioned between ethyl acetate and water (1:1; 100mL) and extracted with ethyl acetate (3×60 mL). The combined organicswere washed with water (3×80 mL), brine (50 mL), dried over magnesiumsulfate, filtered and concentrated in vacuo to give the title compound0.6 g (89% yield) as an orange oil which solidified upon standing.Tr(METCR1278)=1.33 min, (ES⁺) (M+H)⁺ 198.

Step 2, Method 27: [5-(Methoxymethoxy)pyridin-2-yl]methanol

Methyl 5-(methoxymethoxy)pyridine-2-carboxylate (0.39 g, 1.9 mmol) wasdissolved in anhydrous tetrahydrofuran (15 mL) and cooled to 0° C. in anitrogen atmosphere. 2.4 M lithium aluminium hydride in tetrahydrofuran(0.87 mL, 2.09 mmol) was added drop-wise over a period of 5 minutes, andthe reaction was stirred at 0° C. for 1.5 hours. Rochelle's saltsolution (1 mL) was added drop-wise with vigorous stirring over 10minutes and the reaction mixture was warmed to room temperature over 1hour. An emulsion formed which was filtered through paper. The filterpaper was washed with saturated sodium bicarbonate solution (10 mL)followed by ethyl acetate (3×10 mL). The phases were separated and theaqueous was extracted with ethyl acetate (3×10 mL). The combinedorganics were washed with brine (10 mL) and dried over sodium sulfate,filtered and concentrated to give the title compound 276 mg (86% yield)as an orange oil. Tr(METCR1278)=1.09 min, (ES⁺) (M+H)⁺ 170.

Step 3, Method 27: [5-(Methoxymethoxy)pyridin-2-yl]methylmethanesulfonate

[5-(Methoxymethoxy)pyridin-2-yl]methanol (276 mg, 1.63 mmol) wasdissolved in dichloromethane (5 mL), cooled to 0° C. and stirred in anitrogen atmosphere. Triethylamine (250 μL, 1.79 mmol) was added,followed by drop-wise addition of methanesulfonyl chloride (133 μL, 1.71mmol). The reaction was stirred for 45 minutes and warmed roomtemperature. Water (5 mL) was added and the phases separated. Theaqueous layer was extracted with dichloromethane (3×15 mL); the combinedorganic extracts were washed with brine (10 mL), dried over sodiumsulfate, filtered and was concentrated in vacuo to give the titlecompound 275 mg (59% yield) as a dark red oil which was used in the nextstep without further purification. Tr(METCR1278)=1.35 min, (ES⁺) (M+H)⁺248.

Step 4, Method 27:5-{[5-(Methoxymethoxy)pyridin-2-yl]methoxy}-2-(pyridin-3-yl)-1,3-benzoxazole

[5-(Methoxymethoxy)pyridin-2-yl]methyl methanesulfonate (276 mg, 1.11mmol) and 2-(pyridin-3-yl)-1,3-benzoxazol-5-ol (215 mg, 1.01 mmol,prepared by Method 14) were dissolved in anhydrous N,N-dimethylformamide(8 mL) and stirred for 10 minutes in a nitrogen atmosphere at 0° C.Sodium hydride (60% in mineral oil, 122 mg, 3.04 mmol) was added and thereaction mixture stirred for 16 hours. Water (1 mL) was added and thereaction stirred for 10 minutes. The solvents were removed in vacuo andthe residue was partitioned between ethyl acetate (50 mL) and water (20mL). The aqueous was extracted with ethyl acetate (3×50 mL). Thecombined organic extracts were washed with brine (10 mL), dried oversodium sulfate, filtered and concentrated. Purification by FCC (silica,10-100% ethyl acetate in heptane) gave the title compound, 135 mg (36%yield) as a white solid. Tr(METCR1278)=1.78 min, (ES⁺) (M+H)⁺ 364.

Step 5, Method 27:6-({[2-(Pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)pyridin-3-ol

To a solution of5-{[5-(methoxymethoxy)pyridin-2-yl]methoxy}-2-(pyridin-3-yl)-1,3-benzoxazole(135 mg, 0.37 mmol) in tetrahydrofuran (20 mL) was added 3 M aqueoushydrochloric acid (1.3 mL) and the mixture was stirred at 60° C. for 1hour. The reaction was cooled to room temperature and the solventsremoved in vacuo. The residue was diluted with water (10 mL), solidsodium bicarbonate was added until pH 8. The mixture was diluted withwater. The mixture was filtered through paper and collected undersuction to give the title compound 101 mg (85% yield) as a beige solid.

Example 1, Method 27:6-({[2-(Pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)pyridin-3-ol

δ_(H) NMR (500 MHz, DMSO) 9.33 (d, J=2.0 Hz, 1H), 8.80 (dd, J=4.8, 1.5Hz, 1H), 8.51 (dt, J=8.0, 1.9 Hz, 1H), 8.13 (d, J=2.8 Hz, 1H), 7.73 (d,J=8.9 Hz, 1H), 7.65 (dd, J=8.0, 4.8 Hz, 1H), 7.47 (d, J=2.5 Hz, 1H),7.40 (d, J=8.4 Hz, 1H), 7.19 (dd, J=8.4, 2.8 Hz, 1H), 7.12 (dd, J=8.9,2.5 Hz, 1H), 5.12 (s, 2H). Tr(MET-uHPLC-AB-101)=1.91 min, (ES⁺) (M+H)⁺320.

The following example was prepared using Method 27 described above:

TABLE 28 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

319.31 6-({[2-(Pyridin-3- yl)-1,3- benzoxazol-5- yl]oxy}methyl)pyridin-3-ol Tr(MET-uHPLC- AB-101) = 1.91 min, (ES⁺) (M + H)⁺ 320Method 28

Step 1, Method 28: Prop-2-en-1-yl5-(prop-2-en-1-yloxy)pyrazine-2-carboxylate

To sodium hydride (60% in mineral oil, 1.16 g, 29.0 mmol) inN,N-dimethylformamide (25 mL) under nitrogen, was added allyl alcohol(9.90 mL, 144.9 mmol) drop-wise and the mixture stirred at roomtemperature for 20 minutes. A solution of methyl5-chloropyrazine-2-carboxylate (5 g, 29.0 mmol) in N,N-dimethylformamide(25 mL) was added and the mixture stirred at 90° C. for 20 minutes. Themixture was quenched with water (5 mL), diluted with water (200 mL) andextracted with ethyl acetate (2×200 mL). The combined organic extractswere dried over sodium sulfate, filtered and concentrated. Purificationby FCC (silica, 0-30% ethyl acetate in heptane) gave the title compound2.31 g (27% yield) as a light yellow oil. δ_(H) NMR (500 MHz, DMSO) 8.85(s, 1H), 8.45 (s, 111), 6.07 (dddd, J=25.3, 22.6, 10.7, 5.5 Hz, 2H),5.43 (ddd, J=17.2, 9.2, 1.5 Hz, 2H), 5.34-5.25 (m, 2H), 4.94 (d, J=5.5Hz, 2H), 4.83 (d, J=5.5 Hz, 2H). Tr(METCR1278)=1.83 min, (ES⁺) (M+H)⁺221.

Step 2, Method 28: [5-(Prop-2-en-1-yloxy)pyrazin-2-yl]methanol

Sodium borohydride (2.17 g, 57.4 mmol) was added to a stirred solutionof prop-2-en-1-yl 5-(prop-2-en-1-yloxy)pyrazine-2-carboxylate (2.3 g,10.4 mmol) in anhydrous tetrahydrofuran (150 mL) under nitrogen. Themixture was refluxed at 55° C. for 15 minutes then methanol (14 mL,344.6 mmol) was added slowly. The reaction was refluxed at 65° C. for 30minutes then quenched with water (10 mL). The mixture was diluted withwater (200 mL) and extracted with ethyl acetate (2×200 mL). The combinedorganic extracts were dried over sodium sulfate, filtered andconcentrated. Purification by FCC (silica, 20-60% ethyl acetate inheptane) gave the title compound 1.09 g (63% yield) as a colourless oil.δ_(H) NMR (500 MHz, DMSO) 8.25 (s, 1H), 8.19 (s, 1H), 6.07 (ddt, J=16.1,10.6, 5.4 Hz, 1H), 5.44-5.36 (m, 2H), 5.28-5.23 (m, 1H), 4.84 (d, J=5.4Hz, 2H), 4.54 (d, J=5.6 Hz, 2H). Tr(METCR1278)=1.23 min, (ES⁺) (M+H)⁺167.

Step 3, Method 28: [5-(Prop-2-en-1-yloxy)pyrazin-2-yl]methylmethanesulfonate

To a stirred suspension of [5-(prop-2-en-1-yloxy)pyrazin-2-yl]methanol(200 mg, 1.20 mmol) in dichloromethane (10 mL) under nitrogen was addedtriethylamine (0.18 mL, 1.32 mmol). The mixture was cooled to 0° C. andmethanesulfonyl chloride (0.098 mL, 1.26 mmol) was added. The mixturewas warmed to room temperature and stirred for 20 minutes. The mixturewas partitioned between dichloromethane (30 mL) and water (30 mL). Theorganic extract was dried over sodium sulfate, filtered and concentratedto give the title compound 309 mg (quantitative yield) as a yellow oilwhich was used directly in the next step. Tr(METCR1278)=1.61 min, (ES⁺)(M+H)⁺ 245.

Step 4, Method 28:5-{[5-(Prop-2-en-1-yloxy)pyrazin-2-yl]methoxyl}-2-(pyridin-3-yl)-1,3-benzoxazole

To [5-(prop-2-en-1-yloxy)pyrazin-2-yl]methyl methanesulfonate (291 mg,1.19 mmol) and 2-(pyridin-3-yl)-1,3-benzoxazol-5-ol (230 mg, 1.08 mmol,prepared by Method 14) in N,N-dimethylformamide (6 mL) under nitrogen,was added sodium hydride (60% in mineral oil, 48 mg, 1.19 mmol). Themixture was stirred at room temperature overnight. The mixture wasquenched with water (1 mL), diluted with water (30 mL) and extractedwith ethyl acetate (2×30 mL). The combined organic extracts were driedover sodium sulfate, filtered and concentrated. Purification by FCC(silica, 0-2% methanol in dichloromethane) gave the title compound 262mg (67% yield) as an off-white solid. Tr(MET-uHPLC-AB-101)=3.46 min,(ES⁺) (M+H)⁺ 361.

Step 5, Method 28:5-({[2-(Pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)-1,2-dihydropyrazin-2-one

A solution of5-{[5-(prop-2-en-1-yloxy)pyrazin-2-yl]methoxy}-2-(pyridin-3-yl)-1,3-benzoxazole(250 mg, 0.69 mmol) and N,N-dimethyl barbituric acid (108 mg, 0.69 mmol)in N,N-dimethylformamide (10 mL) was degassed with a flow of nitrogenfor 10 minutes. Tetrakis(triphenylphosphine)palladium(0) (16 mg, 0.014mmol) was then added and the mixture was stirred under a nitrogenatmosphere for 1 hour. The mixture was diluted with water (20 mL) andthe precipitate was filtered and dried under vacuum to give the crudeproduct, 186 mg. 50 mg of the crude product was stirred at roomtemperature in dichloromethane (2 mL) for 2 hours. The solid wasfiltered and dried under vacuum to give the title compound 44 mg (20%yield) as an off white powder. Tr(MET-uHPLC-AB-101)=1.86 min, (ES⁺)(M+H)⁺ 321.

Step 6, Method 28:1-Methyl-5-({[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)-1,2-dihydropyrazin-2-one

To a stirred suspension of5-({[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)-1,2-dihydropyrazin-2-one(30 mg, 0.094 mmol) and silver carbonate (65 mg, 0.23 mmol) in anhydroustoluene (2 mL) in a pressure tube was added methyl iodide (0.014 mL,0.22 mmol). The mixture was heated at 100° C. for 2 hours, then at 140°C. for 1 hour. The mixture was diluted with ethyl acetate (10 mL),filtered through glass fibre filterGFF paper and washed with ethylacetate (2×5 mL). The filtrate was concentrated in vacuo and purified bypreparative HPLC (acetonitrile/water) to give the title compound 3.2 mg(10% yield) as an off-white solid.

Example 1, Method 28:1-Methyl-5-({[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)-1,2-dihydropyrazin-2-one

δ_(H) NMR (500 MHz, DMSO) 9.33 (d, J=2.0 Hz, 1H), 8.80 (dd, J=4.8, 1.6Hz, 1H), 8.51 (dt, J=8.0, 1.9 Hz, 1H), 8.06-8.02 (m, 1H), 7.96 (s, 1H),7.74 (d, J=8.9 Hz, 1H), 7.66 (dd, J=8.0, 4.8 Hz, 1H), 7.55 (d, J=2.5 Hz,1H), 7.12 (dd, J=8.9, 2.5 Hz, 1H), 4.97 (s, 2H), 3.46 (s, 3H).Tr(MET-uHPLC-AB-101)=2.03 min, (ES⁺) (M+H)⁺ 335.

The following examples were prepared using Method 28 described above:

TABLE 29 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

334.33 1-methyl-5-({[2- (pyridin-3-yl)-1,3- benzoxazol-5-yl]oxy}methyl)- 1,2- dihydropyrazin-2- one Tr(MET-uHPLC- AB-101) = 2.03min, (ES⁺) (M + H)⁺ 335 2

360.37 5-{[5-(Prop-2-en- 1-yloxy)pyrazin-2- yl]methoxy}-2-(pyridin-3-yl)-1,3- benzoxazole Tr(MET-uHPLC- AB-101) = 1.73 min, (ES⁺)(M + H)⁺ 361 3

320.30 5-({[2-(Pyridin-3- yl)-1,3- benzoxazol-5- yl]oxy}methyl)- 1,2-dihydropyrazin-2- one Tr(MET-uHPLC- AB-101) = 1.86 min, (ES⁺) (M + H)⁺321Method 29

Step 1, Method 29: 5-Methoxy-2-(piperazin-1-yl)pyrimidine

Two microwave tubes were charged with 2-chloro-5-methoxypyrimidine(2×250 mg, 3.46 mmol) and piperazine (2×1.49 g, 34.6 mmol). Isopropanol(2×2.5 mL) was added to each and the reaction mixtures were stirred at140° C. in a microwave for 1 hour. The reaction mixtures were combined,diluted with diethyl ether (50 mL), filtered, the filtrate concentratedand partitioned between water (50 mL) and diethyl ether (50 mL). Theaqueous layer was extracted with diethyl ether (2×50 mL). The combinedorganic extracts were washed with brine (50 mL), dried over magnesiumsulfate, filtered and concentrated to give the title compound 277 mg(32% yield) as a white solid. δ_(H) NMR (500 MHz, chloroform) 8.10 (s,2H), 3.80 (s, 3H), 3.78-3.73 (m, 4H), 3.03-2.93 (m, 4H).

Step 2, Method 29:5-[4-(5-Methoxypyrimidin-2-yl)piperazin-1-yl]-2-(pyridin-3-yl)-1,3-benzoxazole

5-Bromo-2-(pyridin-3-yl)-1,3-benzoxazole (200 mg, 0.73 mmol),5-methoxy-2-(piperazin-1-yl)pyrimidine (180 mg, 0.87 mmol), sodiumtert-butoxide (84 mg, 0.87 mmol) and tetrahydrofuran (5 mL) weredegassed with nitrogen for 20 minutes. Palladium(II) acetate (8 mg, 0.04mmol) and[2′,6′-bis(propan-2-yloxy)biphenyl-2-yl](dicyclohexyl)phosphane (17 mg,0.04 mmol) were added and the reaction mixture was stirred at 70° C. for20 hours. The reaction mixture was cooled to room temperature andpartitioned between ethyl acetate (20 mL) and water (20 mL). The aqueouslayer was extracted with ethyl acetate (2×20 mL). The combined organicextracts were washed with brine (20 mL), dried over magnesium sulfate,filtered and concentrated. Purification by FCC (silica, 25-100% ethylacetate in heptane) and trituration with diethyl ether (5 mL) gave thetitle compound 43 mg (15% yield) as a pale yellow solid.

Example 1, Method 29:5-[4-(5-Methoxypyrimidin-2-yl)piperazin-1-yl]-2-(pyridin-3-yl)-1,3-benzoxazole

δ_(H) NMR (500 MHz, DMSO) 9.32 (d, J=2.1 Hz, 1H), 8.79 (dd, J=4.8, 1.5Hz, 1H), 8.50 (dt, J=8.0, 1.9 Hz, 1H), 8.25 (s, 2H), 7.69 (d, J=9.0 Hz,1H), 7.65 (dd, J=8.0, 4.8 Hz, 1H), 7.38 (d, J=2.3 Hz, 1H), 7.22 (dd,J=9.0, 2.4 Hz, 1H), 3.86-3.80 (m, 4H), 3.79 (s, 3H), 3.27-3.21 (m, 4H).Tr(MET-uHPLC-AB-101)=3.13 min, (ES⁺) (M+H)⁺ 389.

The following example was prepared using Method 29 described above:

TABLE 30 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

388.42 5-[4-(5- Methoxypyrimidin- 2-yl)piperazin-1- yl]-2-(pyridin-3-yl)-1,3- benzoxazole Tr(MET-uHPLC- AB-101) = 3.13 min, (ES⁺) (M + H)⁺389Method 30

Step 1, Method 30: 2-(Pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-ol

2-(Pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-amine (960 mg, 4.52 mmol,prepared by Method 19) was added portion-wise to a stirred solution ofsulphuric acid (4.82 mL, 90.5 mmol) in water (15 mL) at roomtemperature. The solution was cooled to 0-5° C. and a solution of sodiumnitrite (343 mg, 4.98 mmol) in water (10 mL) was added drop-wise. Themixture was stirred for 10 minutes at 0-5° C. A solution of copper(II)nitrate trihydrate (55.1 g, 226.2 mmol) in water (100 mL) was added,followed by copper(I) oxide (647 mg, 4.52 mmol). The mixture was shakenvigorously for 10 minutes. The mixture was basified using saturatedsodium bicarbonate until pH 8-9. 33% Aqueous ammonia (20 mL) was addedand the aqueous solution was extracted with ethyl acetate (2×500 mL).The combined organic extracts were dried over sodium sulfate, filteredand concentrated. Trituration in dichloromethane (10 mL) gave the titlecompound 390 mg (40% yield) as a yellow solid. δ_(H) NMR (500 MHz, DMSO)9.34 (s, 1H), 8.82 (d, J=4.6 Hz, 1H), 8.53 (dt, J=7.9, 1.9 Hz, 1H), 7.96(d, J=2.5 Hz, 1H), 7.66 (dd, J=7.7, 4.7 Hz, 1H), 7.62 (d, J=2.5 Hz, 1H).Tr(METCR1278)=1.25 min, (ES⁺) (M+H)⁺ 214.

Step 2, Method 30:3-{6-[(5-Methoxypyridin-2-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine

To a solution of 2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-ol (50mg, 0.24 mmol) and 2-(chloromethyl)-5-methoxypyridine hydrochloride (46mg, 0.24 mmol) in N,N-dimethylformamide (2 mL) under nitrogen, was addedsodium hydride (60% in mineral oil, 21 mg, 0.52 mmol) and the mixturewas stirred at room temperature overnight. The mixture was quenched withwater (1 mL), diluted with water (15 mL) and extracted with ethylacetate (2×15 mL). The combined organic extracts were dried over sodiumsulfate, filtered and concentrated. Purification by FCC (silica, 0-3%methanol in dichloromethane) followed by preparative HPLC(acetonitrile/water) gave the title compound 29.3 mg (37% yield) as anoff-white powder.

Example 1, Method 30:3-{6-[(5-Methoxypyridin-2-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine

δ_(H) NMR (500 MHz, DMSO) 9.35 (d, J=2.1 Hz, 1H), 8.83 (dd, J=4.8, 1.5Hz, 1H), 8.55 (dt, J=8.0, 1.9 Hz, 1H), 8.31 (d, J=2.9 Hz, 1H), 8.22 (d,J=2.7 Hz, 1H), 8.08 (d, J=2.7 Hz, 1H), 7.67 (dd, J=8.0, 4.8 Hz, 1H),7.57 (d, J=8.6 Hz, 1H), 7.45 (dd, J=8.6, 3.0 Hz, 1H), 5.27 (s, 2H), 3.84(s, 3H). Tr(MET-uHPLC-AB-101)=2.36 min, (ES⁺) (M+H)⁺ 335.

The following example was prepared using Method 30 described above:

TABLE 31 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

334.33 3-{6-[(5- methoxypyridin-2- yl)methoxy}- [1,3]oxazolo[5,4-b]pyridin-2- yl}pyridine Tr(MET-uHPLC- AB-101) = 2.36 min, (ES⁺) (M +H)⁺ 335Method 31

Step 1, Method 31:5-(1-Methyl-1H-pyrazol-4-yl)-2-(pyridin-3-yl)-1,3-benzoxazole

5-Bromo-2-(pyridin-3-yl)-1,3-benzoxazole (300 mg, 1.09 mmol),1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole(250 mg, 1.2 mmol) and 2 M sodium carbonate (1 mL) were suspended inanhydrous N,N-dimethylformamide (10 mL) and sonicated under a flow ofnitrogen for 5 minutes. Tetrakis(triphenylphosphine)palladium(0) (63 mg,0.05 mmol) was added and the reaction mixture was heated to 80° C. for16 hours. The reaction mixture was cooled to room temperature and thesolvents were removed in vacuo. The residue was partitioned betweenethyl acetate (50 mL) and water (30 mL) and the phases separated. Theaqueous was extracted with ethyl acetate (2×30 mL), the combinedorganics were washed with brine solution (5 mL), dried over sodiumsulfate, filtered and concentrated. Purification by FCC (silica, 0-60%ethyl acetate in heptane) gave the title compound, 160 mg (53% yield) asa white solid.

Example 1, Method 31:5-(1-Methyl-1H-pyrazol-4-yl)-2-(pyridin-3-yl)-1,3-benzoxazole

δ_(H) NMR (500 MHz, DMSO) 9.36 (d, J=2.1 Hz, 1H), 8.81 (dd, J=4.8, 1.5Hz, 1H), 8.54 (dt, J=8.0, 1.9 Hz, 1H), 8.22 (s, 1H), 8.04 (d, J=1.5 Hz,1H), 7.96 (s, 1H), 7.80 (d, J=8.5 Hz, 1H), 7.74-7.56 (m, 2H), 3.88 (s,3H). Tr(MET-uHPLC-AB-101)=2.39 min, (ES⁺) (M+H)⁺ 277.

The following example was prepared using Method 31 described above:

TABLE 32 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

276.29 5-(1-Methyl-1H- pyrazol-4-yl)-2- (pyridin-3-yl)-1,3- benzoxazoleTr(MET-uHPLC- AB-101) = 2.39 min, (ES⁺) (M + H)⁺ 277Method 32

Step 1, Method 32: 5-(Chloromethyl)-2-methoxypyridine

To a stirred solution of (6-methoxypyridin-3-yl)methanol (75 mg, 0.54mmol) in dichloromethane (2 mL) under nitrogen was added triethylamine(0.083 mL, 0.59 mmol) followed by methanesulfonyl chloride (0.044 mL,0.57 mmol). The mixture was stirred at room temperature for 1 hour. Themixture was partitioned between dichloromethane (10 mL) and water (10mL). The organic extract was dried over sodium sulfate, filtered andconcentrated to give the title compound 88 mg (quantitative yield) as ayellow oil. Tr(METCR1278)=1.63 min, (ES⁺) (M+H)⁺ 158/160.

Step 2, Method 32:3-{6-[(6-Methoxypyridin-3-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine

To a solution of 2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-ol (90mg, 0.42 mmol, prepared by Method 30) and5-(chloromethyl)-2-methoxypyridine (73 mg, 0.46 mmol) inN,N-dimethylformamide (4 mL) under nitrogen, was added sodium hydride(60% in mineral oil, 19 mg, 0.46 mmol) and the mixture was stirred atroom temperature overnight. The mixture was quenched with water (1 mL),diluted with water (30 mL) and extracted with ethyl acetate (2×30 mL).The combined organic extracts were dried over sodium sulfate, filteredand concentrated. Purification by FCC (silica, 0-3% methanol indichloromethane) and recrystallization from DMSO:acetonitrile (1:1, 10mL) gave the title compound 25.2 mg (18% yield) as an off-white powder.

Example 1, Method 32:3-{6-[(6-Methoxypyridin-3-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine

δ_(H) NMR (500 MHz, DMSO) 9.35 (d, J=2.0 Hz, 1H), 8.83 (dd, J=4.8, 1.6Hz, 1H), 8.55 (dt, J=8.0, 1.9 Hz, 1H), 8.32 (d, J=2.2 Hz, 1H), 8.19 (d,J=2.7 Hz, 1H), 8.10 (d, J=2.7 Hz, 1H), 7.86 (dd, J=8.5, 2.4 Hz, 1H),7.67 (dd, J=8.0, 4.8 Hz, 1H), 6.87 (d, J=8.5 Hz, 1H), 5.22 (s, 2H), 3.86(s, 3H). Tr(MET-uHPLC-AB-101)=2.78 min, (ES⁺) (M+H)⁺ 335.

The following example was prepared using Method 32 described above:

TABLE 33 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

334.33 3-{6-[(6- methoxypyridin-3- yl)methoxy]- [1,3]oxazolo[5,4-b]pyridin-2- yl}pyridine Tr(MET-uHPLC- AB-101) = 2.78 min, (ES⁺) (M +H)⁺ 335Method 33

Step 1, Method 33: 5-Methoxy-2-[4-(methoxymethoxy)phenoxymethyl]pyridine

To a stirred solution of 4-(methoxymethoxy)phenol (1.1 g, 7.13 mmol,described in Journal of Organic Chemistry, 71(22), 2006, 8614) and2-(chloromethyl)-5-methoxypyridine hydrochloride (1.39 g, 7.13 mmol) inN,N-dimethylformamide (40 mL) under nitrogen, was added sodium hydride(60% in mineral oil, 599 mg, 15.0 mmol) and the mixture stirred at roomtemperature for 16 hours. The mixture was then quenched with water (4mL), diluted with water (150 mL) and extracted with ethyl acetate (2×150mL). The combined organic extracts were dried over sodium sulfate,filtered and concentrated to give the title compound 2.2 g (quantitativeyield) as a light brown oil. δ_(H) NMR (500 MHz, DMSO) 8.27 (d, J=2.8Hz, 1H), 7.53-7.34 (m, 2H), 6.94 (s, 4H), 5.09 (s, 2H), 5.04 (s, 2H),3.83 (s, 3H), 3.35 (s, 3H). Tr(METCR1278)=1.71 min, (ES⁺) (M+H)⁺ 276.

Step 2, Method 33: 4-[(5-Methoxypyridin-2-yl)methoxy]phenol

To a solution of 5-methoxy-2-[4-(methoxymethoxy)phenoxymethyl]pyridine(1.96 g, 7.12 mmol) in tetrahydrofuran (100 mL) was added aqueous 3 Mhydrochloric acid (23.4 mL) and the mixture was stirred at roomtemperature overnight. The mixture was then stirred at 40° C. for 5hours. The mixture was diluted with saturated aqueous sodium bicarbonate(200 mL) and extracted with ethyl acetate (2×250 mL). The combinedorganic extracts were dried over sodium sulfate, filtered andconcentrated to give the title compound 1.46 g (87% yield) as a lightpink powder. δ_(H) NMR (500 MHz, DMSO) 8.92 (s, 1H), 8.26 (d, J=2.7 Hz,1H), 7.47-7.37 (m, 2H), 6.86-6.78 (m, 2H), 6.69-6.62 (m, 2H), 4.98 (s,2H), 3.83 (s, 3H). Tr(METCR1278)=1.32 min, (ES⁺) (M+H)⁺ 232.

Step 3, Method 33: 4-[(5-Methoxypyridin-2-yl)methoxy]-2-nitrophenol

To a stirred suspension of 4-[(5-methoxypyridin-2-yl)methoxy]phenol(1.46 g, 6.31 mmol) in 1,2-dimethoxyethane (30 mL) and sulpholane (15mL) at −50° C. under nitrogen was added a suspension of nitroniumtetrafluoroborate (845 mg, 6.31 mmol). The mixture was stirred for 30minutes at −50° C., then slowly warmed to room temperature. The mixturewas concentrated in vacuo and the residue was purified by FCC (silica,20-50% ethyl acetate in heptane then 10% methanol in dichloromethane) togive the title compound 659 mg (33% yield) as a yellow powder. δ_(H) NMR(500 MHz, DMSO) 10.49 (s, 1H), 8.28 (d, J=2.8 Hz, 1H), 7.51 (d, J=3.1Hz, 1H), 7.48 (d, J=8.6 Hz, 1H), 7.42 (dd, J=8.6, 2.9 Hz, 1H), 7.28 (dd,J=9.1, 3.1 Hz, 1H), 7.07 (d, J=9.1 Hz, 1H), 5.09 (s, 2H), 3.83 (s, 3H).Tr(METCR1278)=1.75 min, (ES⁺) (M+H)⁺ 277.

Step 4, Method 33: 2-Amino-4-[(5-methoxypyridin-2-yl)methoxy]phenol

To 4-[(5-methoxypyridin-2-yl)methoxy]-2-nitrophenol (460 mg, 1.66 mmol)and sodium dithionite (1.16 g, 6.66 mmol), was added ethanol (25 mL) andwater (25 mL) and the mixture was stirred at 75° C. for 2.5 hours. Themixture was then treated with sodium dithionite (0.58 g, 3.33 mmol) andthe mixture was stirred at 75° C. for 30 minutes. The mixture wasdiluted with water (150 mL) and extracted with ethyl acetate (2×150 mL).The combined organic extracts were dried over sodium sulfate, filteredand concentrated to give the title compound 292 mg (71% yield) as alight brown solid. 8H NMR (500 MHz, DMSO) 8.49 (s, 1H), 8.25 (t, J=1.8Hz, 1H), 7.40 (d, J=1.8 Hz, 2H), 6.50 (d, J=8.5 Hz, 1H), 6.27 (d, J=2.9Hz, 1H), 6.02 (dd, J=8.5, 2.9 Hz, 1H), 4.91 (s, 2H), 4.55 (s, 2H), 3.82(s, 3H). Tr(METCR1278)=1.23 min, (ES⁺) (M+H)⁺ 247.

Step 5, Method 33:N-{2-Hydroxy-5-[(5-methoxypyridin-2-yl)methoxy]phenyl}-1-methyl-1H-pyrazole-4-carboxamide

To a stirred solution of2-amino-4-[(5-methoxypyridin-2-yl)methoxy]phenol (95 mg, 0.39 mmol) anddiisopropylethylamine (0.077 mL, 0.46 mmol) in tetrahydrofuran (2 mL)under nitrogen, was added 1-methyl-1H-pyrazole-4-carbonyl chloride (60mg, 0.46 mmol) in one portion. The mixture was stirred at roomtemperature for 30 minutes. The mixture was diluted with water (15 mL)and extracted with ethyl acetate (2×15 mL). The combined organicextracts were dried over sodium sulfate, filtered and concentrated togive the title compound 131 mg (96% yield) as a light brown solid.Tr(METCR1278)=1.36 min, (ES⁺) (M+H)⁺ 355.

Step 6, Method 33:5-[(5-Methoxypyridin-2-yl)methoxy]-2-(1-methyl-1H-pyrazol-4-yl)-1,3-benzoxazole

N-{2-Hydroxy-5-[(5-methoxypyridin-2-yl)methoxy]phenyl}-1-methyl-1H-pyrazole-4-carboxamide(65 mg, 0.18 mmol) and acetic acid (1 mL) were heated at 200° C. for 30minutes in a microwave. The mixture was concentrated in vacuo and theresidue was diluted with saturated aqueous sodium bicarbonate solution(20 mL) and extracted with ethyl acetate (2×20 mL). The combined organicextracts were dried over sodium sulfate, filtered and concentrated.Purification by FCC (silica, 20-80% ethyl acetate in heptane) andpreparative HPLC (acetonitrile/water) gave the title compound 36 mg (58%yield) as a white solid.

Example 1, Method 33:5-[(5-Methoxypyridin-2-yl)methoxy]-2-(1-methyl-1H-pyrazol-4-yl)-1,3-benzoxazole

δ_(H) NMR (500 MHz, DMSO) 8.52 (s, 1H), 8.30 (d, J=2.9 Hz, 1H), 8.08 (s,1H), 7.59 (d, J=8.8 Hz, 1H), 7.51 (d, J=8.6 Hz, 1H), 7.43 (dd, J=8.6,3.0 Hz, 1H), 7.33 (d, J=2.5 Hz, 1H), 7.01 (dd, J=8.8, 2.5 Hz, 1H), 5.15(s, 2H), 3.95 (s, 3H), 3.84 (s, 3H). Tr(MET-uHPLC-AB-101)=2.46 min,(ES⁺) (M+H)⁺ 337.

The following examples were prepared using Method 33 described above:

TABLE 34 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

336.34 5-[(5- Methoxypyridin-2- yl)methoxy]-2-(1- methyl-1H-pyrazol-4-yl)-1,3- benzoxazole Tr(MET-uHPLC- AB-101) = 2.46 min, (ES⁺)(M + H)⁺ 337 2

334.33 5-[(5- Methoxypyridin-2- yl)methoxy]-2- (pyrazin-2-yl)-1,3-benzoxazole Tr(MET-uHPLC- AB-101) = 2.42 min, (ES⁺) (M + H)⁺ 335 3

389.45 [(3-{5-[(5- Methoxypyridin-2- yl)methoxy]-1,3- benzoxazol-2-yl}phenyl)methyl] dimethylamine Tr(MET-uHPLC- AB-101) = 1.86 min, (ES⁺)(M + H)⁺ 390Method 34

Step 1, Method 34:N-{2-Hydroxy-5-[(5-methoxypyridin-2-yl)methoxy]phenyl}-1,3-thiazole-5-carboxamide

A stirred solution of 2-amino-4-[(5-methoxypyridin-2-yl)methoxy]phenol(150 mg, 50% purity, 0.30 mmol, prepared by Method 33),1,3-thiazole-5-carboxylic acid (43 mg, 0.33 mmol) and ethylcarbodiimidehydrochloride (76 mg, 0.40 mmol) in pyridine (1 mL) under nitrogen wasstirred at room temperature for 16 hours. The mixture was diluted withwater (10 mL) and extracted with ethyl acetate (2×10 mL). The combinedorganic extracts were dried over sodium sulfate, filtered andconcentrated to give the crude title compound 220 mg as a brown solidwhich was used without further purification. Tr(METCR1278)=1.44 min,(ES⁺) (M+H)⁺ 358.

Step 2, Method 34:5-[(5-Methoxypyridin-2-yl)methoxy]-2-(1,3-thiazol-5-yl)-1,3-benzoxazole

N-{2-Hydroxy-5-[(5-methoxypyridin-2-yl)methoxy]phenyl}-1,3-thiazole-5-carboxamide(109 mg, 0.30 mmol) and acetic acid (2 mL) were heated at 200° C. for 40minutes in a microwave. The mixture was concentrated and the residuediluted with saturated aqueous sodium bicarbonate solution (10 mL) andextracted with ethyl acetate (2×10 mL). The combined organic extractswere dried over sodium sulfate, filtered and concentrated. Purificationby FCC (silica, 25-80% ethyl acetate in heptane) and preparative HPLC(acetonitrile/water) gave the title compound 32 mg (31% yield) as awhite powder.

Example 1, Method 34:5-[(5-Methoxypyridin-2-yl)methoxy]-2-(1,3-thiazol-5-yl)-1,3-benzoxazole

δ_(H) NMR (500 MHz, DMSO) 9.39 (s, 1H), 8.70 (s, 1H), 8.30 (d, J=2.9 Hz,1H), 7.70 (d, J=8.9 Hz, 1H), 7.52 (d, J=8.6 Hz, 1H), 7.46-7.40 (m, 2H),7.12 (dd, J=8.9, 2.6 Hz, 1H), 5.17 (s, 2H), 3.84 (s, 3H).Tr(MET-uHPLC-AB-101)=2.71 min, (ES⁺) (M+H)⁺ 340.

The following examples were prepared using Method 34 described above:

TABLE 35 Mol. Ex. Structure Weight IUPAC Name LCMS data  1

339.37 5-[(5- Methoxypyridin-2- yl)methoxy]-2- (1,3-thiazol-5-yl)-1,3-benzoxazole Tr(MET-uHPLC- AB-101) = 2.71 min, (ES⁺) (M + H)⁺ 340  2

353.41 5-[(5- Methoxypyridin-2- yl)methoxy]-2-(1- methylpiperidin-4-yl)-1,3- benzoxazole Tr(MET-uHPLC- AB-101) = 1.44 min, (ES⁺) (M + H)⁺354  3

407.42 2-[5-(2- Methoxyethoxy) pyridin-3-yl]-5-[(5- methoxypyridin-2-yl)methoxy]-1,3- benzoxazole Tr(MET-uHPLC- AB-101) = 2.85 min, (ES⁺)(M + H)⁺ 408  4

334.34 5-[(5- Methoxypyridin-2- yl)methoxy]-2- (pyrimidin-5-yl)-1,3-benzoxazole Tr(MET-uHPLC- AB-101) = 2.46 min, (ES⁺) (M + H)⁺ 335  5

374.40 2-(2,3-Dihydro-1- benzofuran-2-yl)- 5-[(5- methoxypyridin-2-yl)methoxy]-1,3- benzoxazole Tr(MET-uHPLC- AB-101) = 3.5 min, (ES⁺) (M +H)⁺ 375  6

374.40 2-[(2R)-2,3- Dihydro-1- benzofuran-2-yl]- 5-[(5-methoxypyridin-2- yl)methoxy]-1,3- benzoxazole Tr(MET-uHPLC- AB-101) =3.54 min, (ES⁺) (M + H)⁺ 375  7

374.40 2-[(2S)-2,3- Dihydro-1- benzofuran-2-yl]- 5-[(5-methoxypyridin-2- yl)methoxy]-1,3- benzoxazole Tr(MET-uHPLC- AB-101) =3.55 min, (ES⁺) (M + H)⁺ 375  8

347.37 5-[(5- Methoxypyridin-2- yl)methoxy]-2-(5- methylpyridin-3-yl)-1,3- benzoxazole Tr(MET-uHPLC- AB-101) = 2.89 min, (ES⁺) (M + H)⁺348  9

383.37 5-Phenyl-N-[2- (pyridin-3-yl)-1,3- benzoxazol-5-yl]-1,3,4-oxadiazole-2- carboxamide Tr(MET-uHPLC- AB-101) = 3.04 min, (ES⁺)(M + H)⁺ 384 10

334.34 5-[(5- Methoxypyridin-2- yl)methoxy]-2- (pyrimidin-4-yl)-1,3-benzoxazole Tr(MET-uHPLC- AB-101) = 2.37 min, (ES⁺) (M + H)⁺ 335Method 35

Step 1, Method 35: 2-(Pyridin-2-yloxy)ethan-1-ol

A mixture of sodium hydride (60% in mineral oil, 139 mg, 3.48 mmol) and2-bromopyridine (500 mg, 3.16 mmol) was dissolved inN,N-dimethylformamide (5 mL). Ethane-1,2-diol (2.12 mL, 37.98 mmol) wasadded drop-wise and the mixture heated at 130° C. overnight. The mixturewas cooled to room temperature, water (20 mL) added and the mixtureextracted with ethyl acetate (3×10 mL). The combined organic layers werewashed with water (2×10 mL), dried over sodium sulfate, filtered andconcentrated. Purification by FCC (silica, 2-40% ethyl acetate inheptane) gave the title compound 135 mg (31% yield) as a colorless oil.δ_(H) NMR (500 MHz, chloroform) 8.23-8.06 (m, 1H), 7.61 (ddd, J=9.0,7.1, 2.0 Hz, 1H), 6.91 (ddd, J=7.0, 5.1, 0.8 Hz, 1H), 6.81 (d, J=8.4 Hz,1H), 4.53-4.41 (m, 2H), 4.02-3.90 (m, 2H), 3.81 (br. s, 1H).Tr(METCR1278)=0.59 min, (ES⁺) (M+H)⁺ 140.

Step 2, Method 35: 2-(2-Chloroethoxy)pyridine

To a stirred solution of 2-(pyridin-2-yloxy)ethan-1-ol (56 mg, 0.4 mmol)in dichloromethane (2 mL) under nitrogen at 0° C. was addedtriethylamine (0.06 mL, 0.44 mmol) followed by methanesulfonyl chloride(0.03 mL, 0.42 mmol). The mixture was stirred at room temperature for 2hours. The mixture was cooled to 0° C., triethylamine (0.06 mL, 0.44mmol) and methanesulfonyl chloride (0.03 mL, 0.42 mmol) were added andthe mixture was stirred at room temperature for 4 hours. The mixture waspartitioned between dichloromethane (10 mL) and water (10 mL). Theorganic extract was dried over sodium sulfate, filtered and concentratedto give the crude title compound 58 mg (91% yield) as a yellow oil,which was used directly in the next step.

Step 3, Method 35:5-[2-(Pyridin-2-yloxy)ethoxy]-2-(pyridin-3-yl)-1,3-benzoxazole

To sodium hydride (60% in mineral oil, 12 mg, 0.3 mmol) under nitrogenwas added a solution of 2-(pyridin-3-yl)-1,3-benzoxazol-5-ol (57 mg,0.27 mmol, prepared by Method 14) in N,N-dimethylformamide (1 mL) andthe mixture was stirred at room temperature for 30 minutes. A solutionof 2-(2-chloroethoxy)pyridine (57 mg, 0.36 mmol) inN,N-dimethylformamide (0.5 mL) was added and the mixture was stirred atroom temperature overnight. The mixture was heated to 60° C. for 3hours, cooled to room temperature, sodium hydride (60% in mineral oil,12 mg, 0.3 mmol) was added and the mixture stirred at room temperatureovernight. The mixture was quenched with water (3 mL), extracted withethyl acetate (3×5 mL), the combined organic layers washed with water(2×5 mL), dried over sodium sulfate, filtered and concentrated.Purification by FCC (silica, 1-10% methanol in dichloromethane) andrecrystallisation from tert-butyl methyl ether:ethyl acetate (9:1, 10mL) gave the title compound 15 mg (17% yield) as white crystals.

Example 1, Method 35:5-[2-(Pyridin-2-yloxy)ethoxy]-2-(pyridin-3-yl)-1,3-benzoxazole

δ_(H) NMR (500 MHz, DMSO) 9.32 (d, J=1.6 Hz, 1H), 8.80 (dd, J=4.8, 1.6Hz, 1H), 8.51 (dt, J=8.0, 1.9 Hz, 1H), 7.74 (dd, J=6.8, 1.9 Hz, 1H),7.71 (d, J=8.9 Hz, 1H), 7.65 (dd, J=8.0, 4.8 Hz, 1H), 7.47-7.40 (m, 2H),7.03 (dd, J=8.9, 2.5 Hz, 1H), 6.41 (d, J=8.7 Hz, 1H), 6.24 (td, J=6.7,1.3 Hz, 1H), 4.35-4.26 (m, 4H). Tr(MET-uHPLC-AB-101)=2.25 min, (ES⁺)(M+H)⁺ 334.

The following example was prepared using Method 35 described above:

TABLE 36 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

333.34 5-[2-(Pyridin-2- yloxy)ethoxy]-2- (pyridin-3-yl)-1,3- benzoxazoleTr(MET-uHPLC- AB-101) = 2.25 min, (ES⁺) (M + H)⁺ 334Method 36

Step 1, Method 36: Cert-Butyl 4-methyl-1H-pyrazole-1-carboxylate

To a solution of 4-methyl-1H-pyrazole (3.1 g, 37.8 mol) andN,N-diethylethanamine (10.5 mL, 75.3 mmol) in dichloromethane (100 mL)was added di-tert-butyl dicarbonate (9.1 g, 41.7 mmol) and the mixturewas stirred at room temperature for 6 hours. The mixture was dilutedwith ethyl acetate (300 mL), washed with water (100 mL) and brine (100mL), dried over magnesium sulfate, filtered and concentrated.Purification by FCC (silica, 0-30% ethyl acetate in heptane) gave thetitle compound 5.56 g (81% yield) as a yellow oil. δ_(H) NMR (500 MHz,chloroform) 7.82 (s, 1H), 7.52 (s, 1H), 2.08 (s, 3H), 1.63 (s, 9H).

Step 2, Method 36: tert-Butyl 4-(bromomethyl)-1H-pyrazole-1-carboxylate

A mixture of tert-butyl 4-methyl-1H-pyrazole-1-carboxylate (4 g, 21.95mmol) and N-bromosuccimide (4.3 g, 24.16 mmol) in carbon tetrachloride(50 mL) was heated to 70° C. After addition of2,2′-diazene-1,2-diylbis(2-methylpropanenitrile) (0.5 g, 3.04 mmol) themixture was refluxed for 18 hours. After cooling to room temperature,solids were removed by filtration and the filtrate was concentrated.Purification by FCC (silica, 0-20% ethyl acetate in heptane) gave thetitle compound 2.94 g (43% yield) as a colourless oil. δ_(H) NMR (500MHz, chloroform) 8.10 (s, 1H), 7.73 (s, 1H), 4.39 (s, 2H), 1.65 (s, 9H).Tr(METCR1278)=1.70 min, (ES⁺) (2M+Na)⁺ 545, 92%.

Step 3, Method 36: tert-Butyl4-({[2-(3-cyanopyridin-4-yl)-4,5-dihydro-1-benzofuran-5-yl]oxy}methyl)-1H-pyrazole-1-carboxylate

To a vigorously stirred solution of4-(5-hydroxy-1-benzofuran-2-yl)pyridine-3-carbonitrile (275 mg, 1.16mmol, prepared by Method 9) and tert-butyl4-(bromomethyl)-1H-pyrazole-1-carboxylate (83%, 550 mg, 1.75 mmol) inN,N-dimethylformamide (15 mL) was added potassium iodide (20 mg, 0.12mmol) and sodium hydride (60% in mineral oil, 60 mg, 1.5 mmol). After 2hours the mixture was added to water (100 mL) and brine (100 mL) thenextracted with ethyl acetate (3×100 mL). The combined organic extractswere washed with brine (50 mL), dried over magnesium sulfate, filteredand concentrated. Purification by FCC (silica, 0-80% ethyl acetate inheptane) gave the title compound 259 mg (53% yield). δH _(NMR) (500 MHz,chloroform) 8.93 (s, 1H), 8.83 (d, J=5.3 Hz, 1H), 8.17 (s, 1H), 7.96 (d,J=5.4 Hz, 1H), 7.91 (s, 1H), 7.80 (s, 1H), 7.48 (d, J=9.0 Hz, 1H), 7.17(d, J=2.5 Hz, 1H), 7.08 (dd, J=9.0, 2.6 Hz, 1H), 5.03 (s, 2H), 1.66 (s,9H). Tr(METCR1278)=2.12 min, (ES⁺) (M+Na)⁺ 439.

Step 4, Method 36:4-[5-(1H-Pyrazol-4-ylmethoxy)-1-benzofuran-2-yl]pyridine-3-carbonitrile

To a solution of tert-butyl4-({[2-(3-cyanopyridin-4-yl)-4,5-dihydro-1-benzofuran-5-yl]oxy}methyl)-1H-pyrazole-1-carboxylate(255 mg, 0.61 mmol) in dichloromethane (10 mL) was added trifluoroaceticacid (2 mL) and the mixture was stirred for 3 hours at room temperature.The volatiles were removed in vacuo and the residue was partitionedbetween ethyl acetate (200 mL) and saturated aqueous sodium bicarbonatesolution (100 mL). After separation the organic layer was washed withbrine (50 mL), dried over magnesium sulfate, filtered and concentrated.The residue was triturated with ethyl acetate and heptane to give thetitle compound 132 mg (69% yield) as an off-white, crystalline solid.

Example 1, Method 36:4-[5-(1H-Pyrazol-4-ylmethoxy)-1-benzofuran-2-yl]pyridine-3-carbonitrile

δ_(H) NMR (500 MHz, DMSO) 12.84 (s, 1H), 9.12 (s, 1H), 8.92 (d, J=5.4Hz, 1H), 8.07 (d, J=5.4 Hz, 1H), 7.99-7.91 (m, 1H), 7.88 (s, 1H),7.69-7.56 (m, 2H), 7.47 (d, J=2.6 Hz, 1H), 7.10 (dd, J=9.0, 2.6 Hz, 1H),5.04 (s, 2H). Tr(MET-uHPLC-AB-101)=2.68 min, (ES⁺) (M+H)⁺ 317.

The following example was prepared using Method 36 described above:

TABLE 37 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

316.31 4-[5-(1H-Pyrazol- 4-ylmethoxy)-1- benzofuran-2- yl]pyridine-3-carbonitrile Tr(MET-uHPLC- AB-101) = 2.68 min, (ES⁺) (M + H)⁺ 317Method 37

Step 1, Method 37:1-[5-(Pyridin-3-ylmethoxy)-1-benzofuran-2-yl]ethan-1-one

To a suspension of 3-(bromomethyl)pyridine hydrobromide (861 mg, 3.40mmol), 1-(5-hydroxy-1-benzofuran-2-yl)ethan-1-one (500 mg, 2.84 mmol)and potassium iodide (50 g, 0.3 mmol) in N,N-dimethylformamide (25 mL)at 0° C. was added sodium hydride (60% in mineral oil, 270 mg, 6.75mmol). The ice bath was removed and the mixture was stirred at roomtemperature for 16 hours before being added to brine (100 mL) and water(100 mL). The mixture was extracted with ethyl acetate (3×100 mL), thecombined organic layers washed with brine (50 mL), dried over magnesiumsulfate, filtered and concentrated. Purification by FCC (silica, 20-100%ethyl acetate in heptane) gave the title compound 626 mg (83% yield) asa colourless, crystalline solid. Tr(MET-uHPLC-AB-101)=1.7 min, (ES⁺)(M+H)⁺ 268.

Step 2, Method 37:2,2-Dibromo-1-[5-(pyridin-3-ylmethoxy)-1-benzofuran-2-yl]ethan-1-one

To a suspension of1-[5-(pyridin-3-ylmethoxy)-1-benzofuran-2-yl]ethan-1-one (1.5 g, 5.61mmol) and pyridinium tribromide (2.2 g, 6.9 mmol) in acetic acid (30 mL)was added hydrobromic acid (30% in acetic acid, 1.1 mL) and the mixturewas stirred at room temperature for 18 hours. After removal of thevolatiles in vacuo, the residue was partitioned between ethyl acetate(300 mL) and saturated aqueous sodium bicarbonate (150 mL). The organiclayer was separated, washed with brine (100 mL), dried over magnesiumsulfate, filtered and concentrated. Purification by FCC (silica, 0-100%ethyl acetate in heptane) gave the title compound 472 mg (20% yield) asa colourless solid. δ_(H) NMR (500 MHz, chloroform) 8.72 (s, 1H), 8.61(d, J=3.9 Hz, 1H), 7.81 (d, J=7.8 Hz, 1H), 7.76 (d, J=0.7 Hz, 1H), 7.53(d, J=9.1 Hz, 1H), 7.36 (dd, J=7.8, 4.8 Hz, 1H), 7.24 (dd, J=9.1, 2.6Hz, 1H), 7.19 (d, J=2.5 Hz, 1H), 6.70 (s, 1H), 5.14 (s, 2H).

Step 3, Method 37:3-{[(2-{5H,6H-Imidazo[2,1-b][1,3]thiazol-3-yl}-1-benzofuran-5-yl)oxy]methyl}pyridine

A mixture of2,2-dibromo-1-[5-(pyridin-3-ylmethoxy)-1-benzofuran-2-yl]ethan-1-one(470 mg, 1.11 mmol) and imidazolidine-2-thione (114 mg, 1.12 mmol) inethanol (20 mL) and acetic acid (10 mL) was stirred under reflux for 16hours. The solvent was removed in vacuo and the residue was partitionedbetween ethyl acetate (200 mL) and saturated aqueous sodium bicarbonatesolution (100 mL). The organic layer was washed with brine (50 mL),dried over magnesium sulfate, filtered and concentrated. Purification bySCX column and preparative HPLC (acetonitrile/water+0.2% ammoniumhydroxide) gave the title compound 49 mg (15% yield) as a colourless,crystalline solid.

Example 1, Method 37:3-{[(2-{5H,6H-Imidazo[2,1-b][1,3]thiazol-3-yl}-1-benzofuran-5-yl)oxy]methyl}pyridine

δ_(H) NMR (500 MHz, DMSO) 8.69 (d, J=1.7 Hz, 1H), 8.55 (dd, J=4.8, 1.6Hz, 1H), 7.89 (dd, J=7.8, 1.8 Hz, 1H), 7.52 (d, J=9.0 Hz, 1H), 7.43 (dd,J=7.8, 4.8 Hz, 1H), 7.27 (d, J=2.6 Hz, 1H), 7.17 (s, 1H), 7.05 (dd,J=8.9, 2.6 Hz, 1H), 6.52 (s, 1H), 5.19 (s, 2H), 4.27-3.97 (m, 4H).Tr(MET-uHPLC-AB-101)=1.15 min, (ES⁺) (M+H)⁺ 350.

The following example was prepared using Method 37 described above:

TABLE 38 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

349.41 3-{[(2-{5H,6H- Imidazo[2,1- b][1,3]thiazol-3- yl}-1-benzofuran-5- yl)oxy]methyl} pyridine Tr(MET-uHPLC- AB-101) = 1.15 min, (ES⁺) (M +H)⁺ 350Method 38

Step 1, Method 38:5-[(5-Methoxypyridin-2-yl)methoxy]-2,3-dihydro-1,3-benzoxazole-2-thione

2-Amino-4-[(5-methoxypyridin-2-yl)methoxy]phenol (50% purity, 450 mg,0.91 mmol, prepared by Method 33) and potassium ethyl xanthate (161 mg,1.00 mmol) in ethanol (3 mL) were stirred in a sealed tube at 85° C.overnight. The mixture was concentrated in vacuo to give the titlecompound 263 mg (quantitative yield) as a brown solid.Tr(METCR1278)=1.59 min, (ES⁺) (M+H)⁺ 289.

Step 2, Method 38:2-Chloro-5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazole

To a stirred solution of5-[(5-methoxypyridin-2-yl)methoxy]-2,3-dihydro-1,3-benzoxazole-2-thione(263 mg, 0.91 mmol) in thionyl chloride (1 mL) was addedN,N-dimethylformamide (0.03 mL). The mixture was stirred at 65° C. for 1hour. The mixture was concentrated in vacuo and purified by FCC (silica,10-40% ethyl acetate in heptane) to give the title compound 117 mg (44%yield) as a white solid. δ_(H) NMR (500 MHz, DMSO) 8.29 (d, J=2.9 Hz,1H), 7.67 (d, J=9.0 Hz, 1H), 7.50 (d, J=8.6 Hz, 1H), 7.46-7.38 (m, 2H),7.11 (dd, J=9.0, 2.6 Hz, 1H), 5.16 (s, 2H), 3.83 (s, 3H).Tr(MET-uHPLC-AB-101)=2.92 min, (ES⁺) (M+H)+291/293.

Step 3, Method 38:7-{5-[(5-Methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-5,6,7,8-tetrahydro-1,7-naphthyridine

2-Chloro-5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazole (9 mg, 0.031mmol), 5,6,7,8-tetrahydro-1,7-naphthyridine dihydrochloride (14 mg,0.068 mmol) and 2-propanol (0.4 mL) were heated at 150° C. for 20minutes in a microwave. The mixture was diluted with water (10 mL) andextracted with ethyl acetate (2×10 mL). The combined organic extractswere dried over sodium sulfate, filtered and concentrated. Purificationby FCC (silica, 20-100% ethyl acetate in heptane) gave the titlecompound 5.5 mg (46% yield) as an off-white powder.

Example 1, Method 38:7-{5-[(5-Methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-5,6,7,8-tetrahydro-1,7-naphthyridine

δ_(H) NMR (500 MHz, DMSO) 8.42 (d, J=4.5 Hz, 1H), 8.28 (d, J=2.8 Hz,1H), 7.64 (d, J=7.6 Hz, 1H), 7.47 (d, J=8.6 Hz, 1H), 7.41 (dd, J=8.6,2.9 Hz, 1H), 7.32 (d, J=8.7 Hz, 1H), 7.26 (dd, J=7.6, 4.8 Hz, 1H), 6.99(d, J=2.4 Hz, 1H), 6.67 (dd, J=8.7, 2.5 Hz, 1H), 5.08 (s, 2H), 4.78 (s,2H), 3.91 (t, J=5.9 Hz, 2H), 3.83 (s, 3H), 2.98 (t, J=5.8 Hz, 2H).Tr(MET-uHPLC-AB-101)=2.28 min, (ES⁺) (M+H)⁺ 389.

The following examples were prepared using Method 38 described above:

TABLE 39 Mol. Ex. Structure Weight IUPAC Name LCMS data  1

388.42 7-{5-[(5- Methoxypyridin-2- yl)methoxyl]-1,3- benzoxazol-2-yl}-5,6,7,8-tetrahydro- 1,7-naphthyridine Tr(MET-uHPLC- AB-101) = 2.28 min,(ES⁺) (M + H)⁺ 389  2

322.32 2-(1H-Imidazol-1- yl)-5-[(5- methoxypyridin-2- yl)methoxy]-1,3-benzoxazole Tr(MET-uHPLC- AB-101) = 2.29 min, (ES⁺) (M + H)⁺ 323  3

377.40 2-{5H,6H,7H,8H- Imidazo[1,2- a]pyrazin-7-yl}-5-[(5-methoxypyridin- 2-yl)methoxy]-1,3- benzoxazole Tr(MET-uHPLC- AB-101)= 1.43 min, (ES⁺) (M + H)⁺ 378  4

329.33 2-(3-Fluoroazetidin- 1-yl)-5-[(5- methoxypyridin-2-yl)methoxyl]-1,3- benzoxazole Tr(MET-uHPLC- AB-101) = 2.5 min, (ES⁺)(M + H)⁺ 330  6

377.40 2- {3H,4H,5H,6H,7H- Imidazo[4,5- c]pyridin-5-yl}-5-[(5-methoxypyridin- 2-yl)methoxy]-1,3- benzoxazole Tr(MET-uHPLC- AB-101)= 1.52 min, (ES⁺) (M + H)⁺ 378  8

377.40 5-[(5- Methoxypyridin-2- yl)methoxy]-2- {2H,4H,5H,6H,7H-pyrazolo[4,3- c]pyridin-5-yl}-1,3- benzoxazole Tr(MET-uHPLC- AB-101) =2.18 min, (ES⁺) (M + H)⁺ 378  9

377.40 2-{5H,6H,7H,8H- Imidazo[1,5- a]pyrazin-7-yl}-5-[(5-methoxypyridin- 2-yl)methoxy]-1,3- benzoxazole Tr(MET-uHPLC- AB-101)= 1.45 min, (ES⁺) (M + H)⁺ 378 10

374.39 5-[(5- Methoxypyridin-2- yl)methoxy]-2- {5H,6H,7H- pyrrolo[3,4-b]pyridin-6-yl}-1,3- benzoxazole Tr(MET-uHPLC- AB-101) = 2.47 min, (ES⁺)(M + H)⁺ 375Method 39

Step 1, Method 39: Methyl6-{[(tert-butoxy)carbonyl]amino}pyridine-3-carboxylate

A solution of methyl 6-aminopyridine-3-carboxylate (1 g, 6.57 mmol),di-tert butyl dicarbonate (1.72 g, 7.89 mmol) andN,N-dimethylaminopyridine (56 mg, 0.46 mmol) in tetrahydrofuran (60 mL)was stirred at room temperature overnight. The mixture was concentratedin vacuo to give the title compound 1.79 g (quantitative yield) as alight brown solid. Tr(METCR1278)=1.99 min, (ES⁺) (M+H)⁺ 253.

Step 2, Method 39: 6-{[(tert-Butoxy)carbonyl]amino}pyridine-3-carboxylicacid

To a stirred solution of methyl6-{[(tert-butoxy)carbonyl]amino}pyridine-3-carboxylate (1.66 g, 6.58mmol) in ethanol (75 mL) and tetrahydrofuran (75 mL), was added 2 Nsodium hydroxide (23.0 mL, 46.1 mmol). The mixture was stirred at 55° C.overnight. The mixture was then concentrated to remove ethanol andtetrahydrofuran and the resulting aqueous solution was neutralised using1 N hydrochloric acid (46.1 mL). The resultant precipitate was filteredand dried under vacuum to give the title compound 729 mg (46% yield) asan off-white powder. δ_(H) NMR (500 MHz, DMSO) 13.04 (s, 1H), 10.25 (s,1H), 8.75 (s, 1H), 8.40-8.06 (m, 1H), 7.91 (d, J=7.0 Hz, 1H), 1.48 (s,9H). Tr(METCR1278)=1.57 min, (ES⁺) (M+H)⁺ 239.

Step 3, Method 39: tert-ButylN-[5-({2-hydroxy-5-[(5-methoxypyridin-2-yl)methoxy]phenyl}carbamoyl)pyridin-2-yl]carbamate

A stirred solution of 2-amino-4-[(5-methoxypyridin-2-yl)methoxy]phenol(50% purity, 150 mg, 0.30 mmol, prepared by Method 33),6-{[(tert-butoxy)carbonyl]amino}pyridine-3-carboxylic acid (80 mg, 0.33mmol) and ethylcarbodiimide hydrochloride (76 mg, 0.40 mmol) in pyridine(1 mL) under nitrogen was stirred at room temperature for 16 hours. Themixture was diluted with water (10 mL) and extracted with ethyl acetate(2×10 mL). The combined organic extracts were dried over sodium sulfate,filtered and concentrated to give the title compound 190 mg(quantitative yield) as a light brown solid. Tr(METCR1278)=1.78 min,(ES⁺) (M+H)⁺ 467.

Step 4, Method 39:N-(5-{5-[(5-Methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}pyridin-2-yl)acetamideand5-{5-[(5-Methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}pyridin-2-amine

tert-ButylN-[5-({2-hydroxy-5-[(5-methoxypyridin-2-yl)methoxy]phenyl}carbamoyl)pyridin-2-yl]carbamate(142 mg, 0.30 mmol) and acetic acid (2 mL) were heated at 200° C. for 40minutes in a microwave. The mixture was concentrated and the residue wasdiluted with saturated aqueous sodium bicarbonate solution (20 mL) andextracted with ethyl acetate (2×20 mL). The combined organic extractswere dried over sodium sulfate, filtered and concentrated. Purificationby FCC (silica, 25-80% ethyl acetate in heptane) gaveN-(5-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}pyridin-2-yl)acetamide54 mg (45% yield) as a light pink powder. The fractions containing5-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}pyridin-2-aminewere concentrated and purified by preparative HPLC (acetonitrile/water)to give5-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}pyridin-2-amine2.7 mg (3% yield) as an off-white powder.

Example 1, Method 39:N-(5-{5-[(5-Methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}pyridin-2-yl)acetamide

δ_(H) NMR (500 MHz, DMSO) 10.92 (s, 1H), 9.06 (d, J=2.3 Hz, 1H), 8.48(dd, J=8.8, 2.4 Hz, 1H), 8.33-8.27 (m, 2H), 7.69 (d, J=8.9 Hz, 1H), 7.53(d, J=8.6 Hz, 1H), 7.47-7.41 (m, 2H), 7.10 (dd, J=8.9, 2.5 Hz, 1H), 5.19(s, 2H), 3.84 (s, 3H), 2.16 (s, 3H). Tr(MET-uHPLC-AB-101)=2.66 min,(ES⁺) (M+H)⁺ 391.

Example 2, Method 39:5-{5-[(5-Methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}pyridin-2-amine

δ_(H) NMR (500 MHz, DMSO) 8.70 (d, J=2.3 Hz, 1H), 8.30 (d, J=2.9 Hz,1H), 8.04 (dd, J=8.8, 2.4 Hz, 1H), 7.59 (d, J=8.8 Hz, 1H), 7.51 (d,J=8.6 Hz, 1H), 7.43 (dd, J=8.6, 3.0 Hz, 1H), 7.33 (d, J=2.5 Hz, 1H),6.99 (dd, J=8.8, 2.5 Hz, 1H), 6.81 (s, 2H), 6.58 (d, J=8.8 Hz, 1H), 5.15(s, 2H), 3.83 (s, 3H). Tr(MET-uHPLC-AB-101)=1.76 min, (ES⁺) (M+H)⁺ 349.

The following examples were prepared using Method 39 described above:

TABLE 40 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

390.39 N-(5-{5-[(5- methoxypyridin-2- yl)methoxy]-1,3- benzoxazol-2-yl}pyridin-2- yl)acetamide Tr(MET-uHPLC- AB-101) = 2.66 min, (ES⁺) (M +H)⁺ 391 2

348.36 5-{5-[(5- Methoxypyridin-2- yl)methoxy]-1,3- benzoxazol-2-yl}pyridin-2-amine Tr(MET-uHPLC- AB-101) = 1.76 min, (ES⁺) (M + H)⁺ 349Method 40

Step 1, Method 40: Methyl4-({[tert-butoxy)carbonyl](methyl)amino}methyl)benzoate

To methyl 4-{[(tert-butoxycarbonyl)amino]methyl}benzoate (200 mg, 0.75mmol) and sodium hydride (60% in mineral oil, 32 mg, 0.79 mmol) undernitrogen was added N,N-dimethylformamide (2 mL). The mixture was stirredat room temperature for 10 minutes. Iodomethane (49 μL, 0.79 mmol) wasadded and the mixture was stirred at room temperature for 1 hour. Themixture was diluted with water (20 mL) and extracted with ethyl acetate(2×20 mL). The organic extracts were dried over sodium sulfate, filteredand concentrated. Purification by FCC (silica, 0-40% ethyl acetate inheptane) gave the title compound 151 mg (72% yield) as a light yellowoil. δ_(H) NMR (500 MHz, DMSO) 7.95 (d, J=8.1 Hz, 2H), 7.34 (d, J=8.1Hz, 2H), 4.44 (s, 2H), 3.84 (s, 3H), 2.79 (s, 3H), 1.39 (d, J=43.9 Hz,9H). Tr(METCR1278)=2.03 min, (ES⁺) (M-t-Bu+H)⁺224,(M-t-Bu+acetonitrile)⁺265.

Step 2, Method 40: tert-ButylN-{[4-(hydroxymethyl)phenyl]methyl}-N-methylcarbamate

2.4 M lithium aluminium hydride in tetrahydrofuran (0.23 mL, 0.56 mmol)was added to a stirred solution of methyl4-({[(tert-butoxy)carbonyl](methyl)amino}methyl)benzoate (148 mg, 0.53mmol) in anhydrous tetrahydrofuran (7 mL) under nitrogen. The mixturewas stirred at 0° C. for 30 minutes. The mixture was quenched bycautious addition of water (1 mL) followed by saturated ammoniumchloride solution (0.5 mL). The mixture was stirred at 0° C. for 5minutes. The mixture was diluted with water (20 mL) and extracted withethyl acetate (2×20 mL). The combined organic extracts were dried oversodium sulfate, filtered and concentrated to give the title compound 124mg (93% yield) as a light yellow oil. δ_(H) NMR (500 MHz, DMSO) 7.29 (d,J=7.7 Hz, 2H), 7.16 (d, J=7.8 Hz, 2H), 5.14 (t, J=5.7 Hz, 1H), 4.47 (d,J=5.6 Hz, 2H), 4.34 (s, 2H), 2.73 (s, 3H), 1.41 (d, J=12.9 Hz, 9H).Tr(METCR1278)=1.71 min, (ES⁺) (M+Na)⁺ 273 (M-t-Bu+H)⁺ 196.

Step 3, Method 40: tert-ButylN-({4-[(methanesulfonyloxy)methyl]phenyl}methyl)-N-methylcarbamate

To a stirred solution of tert-butylN-{[4-(hydroxymethyl)phenyl]methyl}-N-methylcarbamate (120 mg, 0.48mmol) in dichloromethane (4 mL) under nitrogen with ice cooling wasadded triethylamine (0.073 mL, 0.52 mmol) followed by methanesulfonylchloride (0.039 mL, 0.50 mmol). The mixture was warmed to roomtemperature and stirred for 2 hours. The mixture was treated withmethanesulfonyl chloride (0.013 mL, 0.17 mmol) and stirred at roomtemperature for 1 hour. The mixture was partitioned betweendichloromethane (20 mL) and water (20 mL). The organic extract was driedover sodium sulfate, filtered and concentrated to give the crude titlecompound 157 mg (57% yield) as a yellow oil which was taken on directlyto the next step. Tr(METCR1278)=1.93 min, (ES⁺) (M+Na)⁺ 352, 57%.

Step 4, Method 40:tert-Butyl-N-methyl-N-{[4-({[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)phenyl]methyl}carbamate

To tert-butylN-({4-[(methanesulfonyloxy)methyl]phenyl}methyl)-N-methylcarbamate (92mg, 0.43 mmol) and 2-(pyridin-3-yl)-1,3-benzoxazol-5-ol (157 mg, 0.48mmol, prepared by Method 14) in N,N-dimethylformamide (3 mL) undernitrogen, was added sodium hydride (60% in mineral oil, 19 mg, 0.48mmol). The mixture was stirred at room temperature overnight. Themixture was then quenched with water (1 mL), diluted with water (30 mL)and extracted with ethyl acetate (2×30 mL). The combined organicextracts were dried over sodium sulfate, filtered and concentrated.Purification by FCC (silica, 20-100% ethyl acetate in heptane) gave thetitle compound 42 mg (22% yield) as an off-white solid. δ_(H) NMR (500MHz, DMSO) 9.33 (d, J=2.1 Hz, 1H), 8.80 (dd, J=4.8, 1.5 Hz, 1H), 8.51(d, J=8.0 Hz, 1H), 7.73 (d, J=8.9 Hz, 1H), 7.65 (dd, J=8.0, 4.8 Hz, 1H),7.51-7.44 (m, 3H), 7.25 (d, J=7.8 Hz, 2H), 7.13 (dd, J=8.9, 2.5 Hz, 1H),5.18 (s, 2H), 4.38 (s, 2H), 2.76 (s, 3H), 1.40 (d, J=23.8 Hz, 9H).Tr(METCR1278)=2.47 min, (ES⁺) (M+H)⁺ 446 (M+Na)⁺468 (M-tBu+H)⁺ 390, 88%.

Step 5, Method 40:Methyl({[4-({[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)phenyl]methyl}amine

To a solution oftert-butyl-N-methyl-N-{[4-({[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)phenyl]methyl}carbamate(40 mg, 0.09 mmol) in dichloromethane (2 mL), was added 4 M hydrogenchloride in 1,4-dioxane (3 mL) and the mixture was stood at roomtemperature for 1 hour. The mixture was concentrated in vacuo andpurified by preparative HPLC (acetonitrile/water+0.2% ammoniumhydroxide) to give the title compound 19.5 mg (63% yield) as anoff-white solid.

Example 1, Method 40:Methyl({[4-({[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)phenyl]methyl)}amine

δ_(H) NMR (500 MHz, DMSO) 9.31 (s, 1H), 8.79 (d, J=3.6 Hz, 1H), 8.50 (t,J=7.5 Hz, 1H), 7.72 (t, J=7.8 Hz, 1H), 7.64 (dd, J=7.8, 5.0 Hz, 1H),7.49-7.45 (m, 1H), 7.42 (d, J=7.9 Hz, 2H), 7.33 (d, J=7.8 Hz, 2H),7.15-7.08 (m, 1H), 5.16 (d, J=4.2 Hz, 2H), 3.63 (s, 2H), 3.23 (br. s,1H), 2.25 (s, 3H). Tr(MET-uHPLC-AB-101)=1.76 min, (ES⁺) (M+H)⁺ 346.

The following example was prepared using Method 40 described above:

TABLE 41 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

345.39 Methyl({[4-({[2- (pyridin-3-yl)-1,3- benzoxazol-5- yl]oxy}methyl)phenyl]methyl}) amine Tr(MET-uHPLC- AB-101) = 1.76 min, (ES⁺) (M + H)⁺346Method 41

Step 1, Method 41:4-{5-[(1-{2-[(tert-Butyldimethylsilyl)oxy]ethyl}-1H-pyrazol-4-yl)methoxy]-1-benzofuran-2-yl}pyridine-3-carbonitrile

To a suspension of4-[5-(1H-pyrazol-4-ylmethoxy)-1-benzofuran-2-yl]pyridine-3-carbonitrile(72 mg, 0.28 mmol, prepared by Method 36),(2-bromoethoxy)(tert-butyl)dimethylsilane (100 mg, 0.42 mmol) andpotassium iodide (10 mg, 0.06 mmol) in N,N-dimethylformamide (5 mL) wasadded sodium hydride (60% in mineral oil, 15 mg, 0.38 mmol) and themixture was stirred at room temperature for 2 hours. The mixture wasadded to water (50 mL) and brine (50 mL) then extracted with ethylacetate (3×50 mL). The combined extracts were washed with brine (50 mL),dried over magnesium sulfate, filtered and concentrated. Purification byFCC (silica, 0-50% ethyl acetate in heptane) gave the title compound 79mg (73% yield) as colourless oil. δ_(H) NMR (500 MHz, chloroform) 8.93(s, 1H), 8.83 (d, J=5.1 Hz, 1H), 7.97 (d, J=5.4 Hz, 1H), 7.92 (s, 1H),7.60 (s, 1H), 7.57 (s, 1H), 7.47 (d, J=9.0 Hz, 1H), 7.19 (d, J=2.5 Hz,1H), 7.08 (dd, J=9.0, 2.6 Hz, 1H), 5.01 (s, 2H), 4.23 (t, J=5.2 Hz, 2H),3.94 (t, J=5.2 Hz, 2H), 0.84 (s, 9H), −0.06 (s, 6H). Tr(METCR1278)=2.52min, (ES⁺) (M+H)⁺ 475.

Step 2, Method 41:4-(5-{[1-(2-Hydroxyethyl)-1H-pyrazol-4-yl]methoxy}-1-benzofuran-2-yl)pyridine-3-carbonitrile

To a solution of4-{5-[(1-{2-[(tert-butyldimethylsilyl)oxy]ethyl}-1H-pyrazol-4-yl)methoxy]-1-benzofuran-2-yl}pyridine-3-carbonitrile(79 mg, 0.17 mmol) in dry tetrahydrofuran (10 mL) at 0° C. was added 1 Mtetrabutylammonium fluoride in tetrahydrofuran (200 μL, 0.2 mmol). Theice bath was removed and the mixture stirred for 3 hours at roomtemperature before being partitioned between ethyl acetate (200 mL) andwater (50 mL). The organic layer was washed with brine (50 mL), driedover magnesium sulfate, filtered and concentrated. Purification by FCC(silica, 0-10% methanol in dichloromethane) gave the title compound 59mg (98% yield) as a colourless crystalline solid.

Example 1, Method 41:4-(5-{[1-(2-Hydroxyethyl)-1H-pyrazol-4-yl]methoxy}-1-benzofuran-2-yl)pyridine-3-carbonitrile

δ_(H) NMR (500 MHz, DMSO) 9.12 (s, 1H), 8.92 (d, J=5.4 Hz, 1H), 8.07 (d,J=5.4 Hz, 1H), 7.95 (s, 1H), 7.84 (s, 1H), 7.62 (d, J=9.0 Hz, 1H), 7.55(s, 1H), 7.47 (d, J=2.6 Hz, 1H), 7.11 (dd, J=9.0, 2.6 Hz, 1H), 5.00 (s,2H), 4.89 (t, J=5.2 Hz, 1H), 4.13 (t, J=5.7 Hz, 2H), 3.80-3.63 (m, 2H).Tr(MET-uHPLC-AB-101)=2.58 min, (ES⁺) (M+H)⁺ 361.

The following examples were prepared using Method 41 described above:

TABLE 42 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

360.37 4-(5-{[1-(2- Hydroxyethyl)-1H- pyrazol-4- yl]methoxy}-1-benzofuran-2- yl)pyridine-3- carbonitrile Tr(MET-uHPLC- AB-101) = 2.58min, (ES⁺) (M + H)⁺ 361 2

374.39 4-(5-{[1-(2- Methoxyethyl)-1H- pyrazol-4- yl]methoxy}-1-benzofuran-2- yl)pyridine-3- carbonitrile Tr(MET-uHPLC- AB-101) = 3.04min, (ES⁺) (M + H)⁺ 375Method 42

Step 1, Method 42:Dimethyl({2-[4-({[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)phenoxy]ethyl})amine

{2-[4-(Chloromethyl)phenoxy]ethyl}dimethylamine hydrochloride (95 mg,0.38 mmol, described in Bioorg. Med. Chem. Lett. 15 (2005) 2891-2893)and 2-(pyridin-3-yl)-1,3-benzoxazol-5-ol (98 mg, 0.38 mmol, prepared byMethod 14) were dissolved in anhydrous N,N-dimethylformamide (5 mL)under nitrogen. Sodium hydride (60% in mineral oil, 46 mg, 1.14 mmol)was added and the mixture stirred at room temperature for 20 hours.Additional sodium hydride (circa 30 mg) was added and the reactionmixture stirred at room temperature for 16 hours. The reaction mixturewas then quenched with water (5 mL) and 2 M sodium hydroxide (5 mL) andthen extracted with ethyl acetate (3×10 mL). The combined organicextracts were washed with brine (10 mL), dried, filtered andconcentrated. Purification by preparative HPLC (acetonitrile/water+0.2%ammonium hydroxide) gave the title compound 9.2 mg (6% yield) as a whitepowder.

Example 1 Method 42:Dimethyl({2-[4-({[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)phenoxy]ethyl})amine

δ_(H) NMR (500 MHz, DMSO) 9.33 (d, J=2.0 Hz, 1H), 8.80 (dd, J=4.8, 1.6Hz, 1H), 8.51 (dt, J=8.0, 1.9 Hz, 1H), 7.72 (d, J=8.9 Hz, 1H), 7.65 (dd,J=8.0, 4.8 Hz, 1H), 7.47 (d, J=2.5 Hz, 1H), 7.41 (d, J=8.6 Hz, 2H), 7.10(dd, J=8.9, 2.5 Hz, 1H), 6.96 (d, J=8.6 Hz, 2H), 5.10 (s, 2H), 4.04 (t,J=5.8 Hz, 2H), 2.61 (t, J=5.8 Hz, 2H), 2.20 (s, 6H).Tr(MET-uHPLC-AB-101)=1.91 min, (ES⁺) (M+H)⁺ 390.

The following example was prepared using Method 42 described above:

TABLE 43 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

389.45 Dimethyl({2-[4- ({[2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]oxy}methyl) phenoxy]ethyl}) amine Tr(MET-uHPLC- AB-101) = 1.91 min,(ES⁺) (M + H)⁺ 390Method 43

Step 1, Method 43: Methyl 5-(2-methoxyethoxy)pyridine-2-carboxylate

To sodium hydride (60% in mineral oil, 131 mg, 3.26 mmol) and methyl5-hydroxypyridine-2-carboxylate (500 mg, 3.27 mmol) under nitrogen wasadded anhydrous N,N-dimethylformamide (5 mL) and the mixture stirred atroom temperature for 15 minutes. A solution of 1-bromo-2-methoxyethane(477 mg, 3.43 mmol) in N,N-dimethylformamide (5 mL) was added slowly.The mixture was stirred at room temperature overnight and then heated at65° C. for 3.5 hours. The mixture was diluted with water (50 mL) andextracted with ethyl acetate (2×50 mL). The combined organic extractswere dried over sodium sulfate, filtered and concentrated to give thetitle compound 688 mg (quantitative yield) as a light brown oil. δ_(H)NMR (500 MHz, DMSO) 8.39 (d, J=2.9 Hz, 1H), 8.03 (d, J=8.7 Hz, 1H), 7.53(dd, J=8.7, 2.9 Hz, 1H), 4.31-4.23 (m, 2H), 3.84 (s, 3H), 3.72-3.66 (m,2H), 3.31 (s, 3H). Tr(METCR1278)=1.25 min, (ES⁺) (M+H)⁺ 212.

Step 2, Method 43: [5-(2-Methoxyethoxy)pyridin-2-yl]methanol

Lithium aluminium hydride (2.4 M in tetrahydrofuran, 0.93 mL, 2.22 mmol)was added to a stirred solution of methyl5-(2-methoxyethoxy)pyridine-2-carboxylate (148 mg, 0.53 mmol) inanhydrous tetrahydrofuran (35 mL) under nitrogen. The mixture wasstirred at 0° C. for 30 minutes. The mixture was then quenched bycautious addition of water (2 mL) followed by saturated ammoniumchloride solution (1 mL). The mixture was stirred at 0° C. for 5 minutesthen diluted with water (100 mL), extracted with ethyl acetate (2×100mL). The combined organic extracts were dried over sodium sulfate,filtered and concentrated to give the title compound 243 mg (63% yield)as a transparent oil. δ_(H) NMR (500 MHz, DMSO) 8.18 (d, J=2.7 Hz, 1H),7.41-7.34 (m, 2H), 5.28 (t, J=5.7 Hz, 1H), 4.48 (d, J=5.1 Hz, 2H), 4.15(dd, J=5.3, 3.7 Hz, 2H), 3.69-3.61 (m, 2H), 3.30 (s, 3H).Tr(METCR1278)=solvent front, (ES⁺) (M+H)⁺ 184.

Step 3, Method 43: [5-(2-Methoxyethoxy)pyridin-2-yl]methylmethanesulfonate

To a stirred solution of [5-(2-methoxyethoxy)pyridin-2-yl]methanol (88mg, 0.48 mmol) in dichloromethane (3 mL) under nitrogen at 0° C., wasadded triethylamine (0.07 mL, 0.53 mmol) followed by methanesulfonylchloride (0.04 mL, 0.5 mmol) and the mixture stirred at room temperaturefor 2 hours. The mixture was then partitioned between dichloromethane(10 mL) and water (10 mL). The organic extract was dried over sodiumsulfate, filtered and concentrated to give the title compound 119 mg(95% yield) as a brown oil which was used in the next step.

Step 4, Method 43:5-{[5-(2-Methoxyethoxy)pyridin-2-yl]methoxy}-2-(pyridin-3-yl)-1,3-benzoxazole

To sodium hydride (60% in mineral oil, 21 mg, 0.53 mmol) under nitrogen,was added a solution of 2-(pyridin-3-yl)-1,3-benzoxazol-5-ol (102 mg,0.48 mmol prepared by Method 14) in N,N-dimethylformamide (2 mL) and themixture was stirred at room temperature for 30 minutes. After that, asolution of [5-(2-methoxyethoxy)pyridin-2-yl]methyl methanesulfonate(125 mg, 0.48 mmol) in N,N-dimethylformamide (1 mL) was added and themixture was left stirring at room temperature overnight. Sodium hydride(60% in mineral oil, 21 mg, 0.53 mmol) and potassium iodide (8 mg, 0.05mmol) were added and the mixture was stirred at room temperature for 2hours. The mixture was then quenched with water (8 mL) extracted withethyl acetate (2×5 mL) and the combined organic extracts washed withwater (4×5 mL), dried over sodium sulfate, filtered and evaporated.Purification by FCC (silica, 0-10% methanol in dichloromethane) andrecrystallisation from tert-butyl methyl ether (9 mL) gave the titlecompound 31 mg (17% yield) as a white powder.

Example 1, Method 43:5-{[5-(2-Methoxyethoxy)pyridin-2-yl]methoxy}-2-(pyridin-3-yl)-1,3-benzoxazole

δ_(H) NMR (500 MHz, DMSO) 9.33 (d, J=2.1 Hz, 1H), 8.80 (dd, J=4.8, 1.6Hz, 1H), 8.51 (dt, J=8.0, 1.9 Hz, 1H), 8.31 (d, J=2.9 Hz, 1H), 7.74 (d,J=8.9 Hz, 1H), 7.65 (dd, J=8.0, 4.8 Hz, 1H), 7.55-7.42 (m, 3H), 7.14(dd, J=8.9, 2.5 Hz, 1H), 5.19 (s, 2H), 4.23-4.15 (m, 2H), 3.70-3.63 (m,2H), 3.31 (s, 3H). Tr(MET-uHPLC-AB-101)=2.61 min, (ES⁺) (M+H)⁺ 378.

The following example was prepared using Method 43 described above:

TABLE 44 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

377.39 5-{[5-2- Methoxyethoxy) pyridin-2-yl] methoxy}-2- (pyridin-3-yl)-1,3-benzoxazole Tr(MET-uHPLC- AB-101) = 2.61 min, (ES⁺) (M + H)⁺ 378Method 44

Step 1, Method 44:4-(5-{[1-(2-Oxoethyl)-1H-pyrazol-4-yl]methoxy}-1-benzofuran-2-yl)pyridine-3-carbonitrile

To a solution of4-(5-{[1-(2-hydroxyethyl)-1H-pyrazol-4-yl]methoxy}-1-benzofuran-2-yl)pyridine-3-carbonitrile(48 mg, 0.13 mmol, prepared by Method 41) in dichloromethane (10 mL) wasadded 1,1,1-triacetoxy-1,1-dihydro-1,2-benziodoxol-3(1H)-one (57 mg,0.13 mmol) and the mixture was stirred for 4 hours at room temperature.1,1,1-Triacetoxy-1,1-dihydro-1,2-benziodoxol-3(1H)-one (57 mg, 0.13mmol) was added and stirring was continued for 12 hours.1,1,1-Triacetoxy-1,1-dihydro-1,2-benziodoxol-3(1H)-one (57 mg, 0.13mmol) was added and the mixture was stirred for 2 hours. The mixture wasdiluted with ethyl acetate (200 mL) then washed with saturated aqueoussodium bicarbonate solution, 10% aqueous sodium thiosulfate solution (50mL, 1:1) and brine (50 mL). The organic phase was dried over magnesiumsulfate, filtered and concentrated. Purification by FCC (silica, 0-10%methanol in dichloromethane) gave the title compound 43 mg (90% yield)as a colourless resin. Tr(METCR1278)=1.62 min, (ES⁺) (M+H)⁺ 377.

Step 2, Method 44:4-[5-({1-[2-(Dimethylamino)ethyl]-1H-pyrazol-4-yl}methoxy)-1-benzofuran-2-yl]pyridine-3-carbonitrile

To a solution of4-(5-{[1-(2-oxoethyl)-1H-pyrazol-4-yl]methoxy}-1-benzofuran-2-yl)pyridine-3-carbonitrile(40 mg, 0.11 mmol), 2 M dimethylamine in methanol (0.170 mL, 0.34 mmol)and acetic acid (50 μL, 0.87 mmol) in dichloromethane was added sodiumtriacetoxyborohydride (80 mg, 0.38 mmol) and the mixture was stirred atroom temperature for 18 hours. The mixture was partitioned between ethylacetate (150 mL) and saturated aqueous sodium bicarbonate solution (50mL). After separation the organic layer was washed with brine (50 mL),dried over magnesium sulfate, filtered and concentrated. Purification bypreparative HPLC (acetonitrile/water+0.2% ammonium hydroxide) gave thetitle compound 15.8 mg (37% yield) as a yellow gum.

Example 1, Method 44:4-[5-({1-[2-(Dimethylamino)ethyl]-1H-pyrazol-4-yl}methoxy)-1-benzofuran-2-yl]pyridine-3-carbonitrile

δ_(H) NMR (500 MHz, DMSO) 9.12 (s, 1H), 8.92 (d, J=5.4 Hz, 1H), 8.07 (d,J=5.4 Hz, 1H), 7.95 (s, 1H), 7.87 (s, 1H), 7.62 (d, J=9.0 Hz, 1H), 7.53(s, 1H), 7.46 (d, J=2.6 Hz, 1H), 7.11 (dd, J=9.0, 2.6 Hz, 1H), 5.00 (s,2H), 4.17 (t, J=6.5 Hz, 2H), 2.62 (t, J=6.5 Hz, 2H), 2.15 (s, 6H).Tr(MET-uHPLC-AB-101)=1.85 min, (ES⁺) (M+H)⁺ 388.

The following example was prepared using Method 44 described above:

TABLE 45 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

387.43 4-[5-({1-[2- (Dimethylamino) ethyl]-1H-pyrazol- 4-yl}methoxy)-1-benzofuran-2- yl]pyridine-3- carbonitrile Tr(MET-uHPLC- AB-101) = 1.85min, (ES⁺) (M + H)⁺ 388Method 45

Step 1, Method 45: 6-(Methylamino)pyridine-3-carboxylic acid

To a solution of 6-(methylamino)pyridine-3-carbonitrile (1.0 g, 7.51mmol) in ethanol (20 mL) and tetrahydrofuran (20 mL) was added sodiumhydroxide (2.4 g, 60.0 mmol) and the mixture was stirred under refluxfor 16 hours. After cooling the solid was collected, washed with ethylacetate (50 mL) and dried under vacuum. The solid was taken up in water(30 mL) and then acidified with 1 N hydrochloric acid to pH 3. Afterdilution with tetrahydrofuran (300 mL) and washing with brine (50 mL),the solution was dried over magnesium sulfate, filtered and concentratedto give the title compound 1.2 g (84% yield, 80% NMR purity) as anoff-white solid. δ_(H) NMR (500 MHz, DMSO) 12.80 (s, 1H), 8.44 (s, 2H),7.93 (d, J=8.7 Hz, 1H), 6.77 (d, J=8.6 Hz, 1H), 2.92 (s, 3H).

Steps 2 and 3, Method 45:5-{5-[(5-Methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-N-methylpyridin-2-amine

To a solution of 2-amino-4-[(5-methoxypyridin-2-yl)methoxy]phenol (50%pure, 125 mg, 0.25 mmol, prepared by Method 33) and6-(methylamino)pyridine-3-carboxylic acid (80% pure, 63 mg, 0.33 mmol)in pyridine (2 mL) was added1-(3-(dimethylamino)-propyl)-3-ethylcarbodiimide hydrochloride (70 mg,0.37 mmol) and the mixture was stirred at room temperature for 18 hours.The solvent was removed in vacuo and the residue was taken up in ethylacetate (200 mL). The solution was washed with water (50 mL) and brine(50 mL). The organic extract was dried over magnesium sulfate, filteredand concentrated. This was taken up in acetic acid (3 mL) and heated ina microwave at 200° C. for 40 minutes. After cooling the volatiles wereremoved in vacuo and the residue was partitioned between ethyl acetate(200 mL) and saturated aqueous sodium bicarbonate solution (100 mL). Theorganic layer was washed with brine (50 mL), dried over magnesiumsulfate, filtered and then pre-absorbed onto a small amount of silica.Purification by FCC (silica, 0-10% methanol in dichloromethane) andpreparative HPLC (acetonitrile/water) gave the title compound 9.9 mg(17% yield) as an off-white solid.

Example 1, Method 45:5-{5-[(5-Methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-N-methylpyridin-2-amine

δ_(H) NMR (500 MHz, DMSO) 8.77 (d, J=2.2 Hz, 1H), 8.30 (d, J=2.9 Hz,1H), 8.03 (d, J=7.6 Hz, 1H), 7.59 (d, J=8.8 Hz, 1H), 7.51 (d, J=8.6 Hz,1H), 7.42 (dd, J=8.6, 2.9 Hz, 1H), 7.39-7.34 (m, 1H), 7.33 (d, J=2.5 Hz,1H), 6.99 (dd, J=8.8, 2.5 Hz, 1H), 6.60 (d, J=8.9 Hz, 1H), 5.15 (s, 2H),3.83 (s, 3H), 2.86 (d, J=4.8 Hz, 3H). Tr(MET-uHPLC-AB-101)=1.98 min,(ES⁺) (M+H)⁺ 363.

The following examples were prepared using Method 45 described above:

TABLE 46 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

362.38 5-{5-[(5- Methoxypyridin-2- yl)methoxy]-1,3- benzoxazol-2-yl}-N-methylpyridin-2- amine Tr(MET-uHPLC- AB-101) = 1.98 min, (ES⁺) (M +H)⁺ 363 2

347.37 5-[(5- Methoxypyridin-2- yl)methoxy]-2-(2- methylpyridin-4-yl)-1,3- benzoxazole Tr(MET-uHPLC- AB-101) = 2.4 min, (ES⁺) (M + H)⁺ 3483

424.46 5-[(5- Methoxypyridin-2- yl)methoxy]-2-(3- phenoxyphenyl)-1,3-benzoxazole Tr(MET-uHPLC- AB-101) = 4.47 min, (ES⁺) (M + H)⁺ 425 4

364.36 6-{5-[(5- Methoxypyridin-2- yl)methoxy]-1,3- benzoxazol-2-yl}-2-methyl-2,3- dihydropyridazin- 3-one Tr(MET-uHPLC- AB-101) = 2.58 min,(ES⁺) (M + H)⁺ 365 5

334.34 5-[(5- Methoxypyridin-2- yl)methoxy]-2- (pyridazin-3-yl)-1,3-benzoxazole Tr(MET-uHPLC- AB-101) = 2.21 min, (ES⁺) (M + H)⁺ 335 6

334.34 5-[(5- Methoxypyridin-2- yl)methoxy]-2- (pyridazin-4-yl)-1,3-benzoxazole Tr(MET-uHPLC- AB-101) = 2.33 min, (ES⁺) (M + H)⁺ 335Method 46

Step 1, Method 46:3-{[(2-{5H,6H-Imidazo[2,1-b][1,3]thiazol-3-yl}-1-benzofuran-5-yl)oxy]methyl}pyridine

To a solution of3-{[(2-{5H,6H-imidazo[2,1-b][1,3]thiazol-3-yl}-1-benzofuran-5-yl)oxy]methyl}pyridine(30 mg, 0.086 mmol, prepared by Method 37) in dichloromethane at 0° C.was added 0.43 M bromine in dichloromethane (0.2 mL, 0.086 mmol). Afterremoval of the ice-bath the mixture was stirred for 1 hour at roomtemperature before being diluted with ethyl acetate. The solid wascollected by filtration and then dried under vacuum. Purification bypreparative HPLC (acetonitrile/water+0.2% ammonium hydroxide) gave thetitle compound 9.9 mg (27% yield) as an off-white solid.

Example 1, Method 46:3-{[(2-{2-Bromo-5H,6H-imidazo[2,1-b][1,3]thiazol-3-yl}-1-benzofuran-5-yl)oxy]methyl}pyridine

δ_(H) NMR (500 MHz, DMSO) 8.70 (d, J=1.8 Hz, 1H), 8.55 (dd, J=4.8, 1.6Hz, 1H), 7.94-7.85 (m, 1H), 7.57 (d, J=9.0 Hz, 1H), 7.49-7.40 (m, 2H),7.36 (d, J=2.6 Hz, 1H), 7.11 (dd, J=9.0, 2.6 Hz, 1H), 5.20 (s, 2H),4.15-4.00 (m, 4H). Tr(MET-uHPLC-AB-101)=1.36 min, (ES⁺) (M+H)⁺ 428/430.

The following example was prepared using Method 46 described above:

TABLE 47 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

428.30 3-{[(2-{2-Bromo- 5H,6H- imidazo[2,1-b] [1,3]thiazol-3-yl}-1-benzofuran- 5-yl)oxy] methyl}pyridine Tr(MET-uHPLC- AB-101) = 1.36min, (ES⁺) (M + H)⁺ 428/430Method 47

Step 1, Method 47: 5-[(5-Methoxypyrazin-2-yl)methoxy]-2-nitroaniline

To a stirred solution of 3-amino-4-nitrophenol (220 mg, 1.43 mmol) inN,N-dimethylformamide (5 mL) under nitrogen was added potassiumtert-butoxide (160 mg, 1.42 mmol) and the mixture stirred for 5 minutesat room temperature. A solution of (5-methoxypyrazin-2-yl)methylmethanesulfonate (311 mg, 1.43 mmol, prepared by Method 20) inN,N-dimethylformamide (3 mL) was added and the mixture was stirred atroom temperature for 16 hours. The mixture was diluted with water (100mL) and extracted with ethyl acetate (2×100 mL). The combined organicextracts were washed with 0.2 M sodium hydroxide (3×50 mL), dried oversodium sulfate, filtered and concentrated to give the title compound 213mg (54% yield) as a bright yellow solid. δ_(H) NMR (500 MHz, DMSO)8.39-8.30 (m, 2H), 7.53 (d, J=3.0 Hz, 1H), 7.28 (s, 2H), 7.24 (dd,J=9.2, 3.0 Hz, 1H), 7.01 (d, J=9.2 Hz, 1H), 5.10 (s, 2H), 3.92 (s, 3H).Tr(METCR1278)=1.72 min, (ES⁺) (M+H)⁺ 277.

Step 2, Method 47:N-{5-[(5-Methoxypyrazin-2-yl)methoxy]-2-nitrophenyl}pyridine-3-carboxamide

To a stirred solution of5-[(5-methoxypyrazin-2-yl)methoxy]-2-nitroaniline (213 mg, 0.77 mmol) intetrahydrofuran (8 mL), was added diisopropylethylamine (0.16 mL, 0.92mmol) followed by pyridine-3-carbonyl chloride hydrochloride (144 mg,0.81 mmol). The mixture was stirred at room temperature overnight. Themixture was diluted with water (30 mL) and saturated aqueous sodiumbicarbonate solution (10 mL) and extracted with ethyl acetate (2×50 mL).The combined organic extracts were dried over sodium sulfate, filteredand concentrated to give the title compound 239 mg (81% yield) as abright yellow solid. δ_(H) NMR (500 MHz, DMSO) 10.74 (s, 1H), 9.10 (d,J=2.1 Hz, 1H), 8.73 (d, J=4.6 Hz, 1H), 8.42 (d, J=1.2 Hz, 1H), 8.35 (d,J=1.4 Hz, 1H), 8.27 (dt, J=7.9, 1.9 Hz, 1H), 7.65 (d, J=8.9 Hz, 1H),7.61 (s, 1H), 7.54 (dd, J=8.6, 4.0 Hz, 1H), 7.39 (d, J=8.7 Hz, 1H), 5.25(s, 2H), 3.93 (s, 3H). Tr(METCR1278)=1.72 min, (ES⁺) (M+H)⁺ 382.

Step 3, Method 47:5-[(5-Methoxypyrazin-2-yl)methoxy]-2-(pyridin-3-yl)-1H-1,3-benzodiazole

To a stirred suspension ofN-{5-[(5-methoxypyrazin-2-yl)methoxy]-2-nitrophenyl}pyridine-3-carboxamide(239 mg, 0.63 mmol) in acetic acid (4 mL) and ethanol (2 mL), was addediron powder (262 mg, 4.70 mmol). The mixture was stirred at 78° C. for1.5 hours. The mixture was filtered through glass fibre filter paper andthe filtrate was concentrated in vacuo. Purification by FCC (silica,0-10% methanol in dichloromethane) and preparative HPLC(acetonitrile/water+0.2% ammonium hydroxide) gave the title compound 52mg (25% yield) as an off-white crystalline solid. δ_(H) NMR (500 MHz,DMSO) 12.97 (s, 1H), 9.30 (d, J=1.9 Hz, 1H), 8.65 (d, J=4.8 Hz, 1H),8.44 (d, J=8.0 Hz, 1H), 8.41 (s, 1H), 8.35 (s, 1H), 7.60-7.51 (m, 2H),7.24 (s, 1H), 6.96 (dd, J=8.7, 2.3 Hz, 1H), 5.21 (s, 2H), 3.92 (s, 3H).Tr(MET-uHPLC-AB-101)=1.74 min, (ES⁺) (M+H)⁺ 334.

Step 4, Method 47:6-[(5-Methoxypyrazin-2-yl)methoxy]-1-methyl-2-(pyridin-3-yl)-1H-1,3-benzodiazoleand5-[(5-Methoxypyrazin-2-yl)methoxy]-1-methyl-2-(pyridin-3-yl)-1H-1,3-benzodiazole

5-[(5-Methoxypyrazin-2-yl)methoxy]-2-(pyridin-3-yl)-1H-1,3-benzodiazole(40 mg, 0.12 mmol) was dissolved in acetone (1 mL) under nitrogen, andpowdered potassium hydroxide (34 mg, 0.6 mmol) was added, followed by asolution of methyl iodide (0.007 mL, 0.12 mmol) in acetone (1 mL). Themixture was stirred at room temperature for 2 hours. The mixture wasdiluted with water (20 mL) and extracted with ethyl acetate (2×20 mL).The combined organic extracts were dried over sodium sulfate, filteredand concentrated. Purification by preparative HPLC(acetonitrile/water+0.1% formic acid) gave5-[(5-methoxypyrazin-2-yl)methoxy]-1-methyl-2-(pyridin-3-yl)-1H-1,3-benzodiazole5.8 mg (14% yield) and6-[(5-methoxypyrazin-2-yl)methoxy]-1-methyl-2-(pyridin-3-yl)-1H-1,3-benzodiazole10.1 mg (24% yield), as off-white powders.

Example 1, Method 47:5-[(5-Methoxypyrazin-2-yl)methoxy]-1-methyl-2-(pyridin-3-yl)-1H-1,3-benzodiazole

δ_(H) NMR (500 MHz, DMSO) 9.04 (s, 1H), 8.73 (d, J=3.8 Hz, 1H), 8.40 (d,J=1.0 Hz, 1H), 8.34 (d, J=1.3 Hz, 1H), 8.26 (dt, J=7.9, 1.7 Hz, 1H),7.60 (dd, J=7.9, 4.6 Hz, 1H), 7.56 (d, J=8.8 Hz, 1H), 7.37 (d, J=2.3 Hz,1H), 7.05 (dd, J=8.8, 2.3 Hz, 1H), 5.21 (s, 2H), 3.92 (s, 3H), 3.88 (s,3H). Tr(MET-uHPLC-AB-101)=1.70 min, (ES⁺) (M+H)⁺ 348.

Example 2, Method 47:6-[(5-Methoxypyrazin-2-yl)methoxy]-1-methyl-2-(pyridin-3-yl)-1H-1,3-benzodiazole

δ_(H) NMR (500 MHz, DMSO) 9.04 (s, 1H), 8.73 (s, 1H), 8.45-8.41 (m, 1H),8.35 (d, J=1.3 Hz, 1H), 8.25 (d, J=7.9 Hz, 1H), 7.64-7.58 (m, 2H), 7.38(d, J=2.3 Hz, 1H), 6.98 (dd, J=8.7, 2.4 Hz, 1H), 5.25 (s, 2H), 3.93 (s,3H), 3.88 (s, 3H). Tr(MET-uHPLC-AB-101)=1.74 min, (ES⁺) (M+H)⁺ 348.

The following examples were prepared using Method 47 described above:

TABLE 48 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

347.37 5-[(5- Methoxypyrazin-2- yl)methoxy]-1- methyl-2-(pyridin-3-yl)-1H-1,3- benzodiazole Tr(MET-uHPLC- AB-101) = 1.7 min, (ES⁺) (M +H)⁺ 348 2

347.37 6-[(5- Methoxypyrazin-2- yl)methoxy]-1- methyl-2-(pyridin-3-yl)-1H-1,3- benzodiazole Tr(MET-uHPLC- AB-101) = 1.74 min, (ES⁺) (M +H)⁺ 348 3

333.34 5-[(5- Methoxypyrazin-2- yl)methoxy]-2- (pyridin-3-yl)-1H-1,3-benzodiazole Tr(MET-uHPLC- AB-101) = 1.74 min, (ES⁺) (M + H)⁺ 334Method 48

Step 1, Method 48:5-[(5-Methoxypyridin-2-yl)methoxy]-2-(piperazin-1-yl)-1,3-benzoxazole

tert-Butyl4-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}piperazine-1-carboxylate(50 mg, 0.11 mmol, prepared by Method 38) was stirred in 4 M hydrogenchloride in 1,4-dioxane (1 mL) for 2 hours. The reaction mixture wasdiluted with water (10 mL) and solid sodium bicarbonate was addedportionwise (until pH 8). The solution was extracted withdichloromethane (3×10 mL), and the combined organic extracts were washedwith brine (10 mL), dried over sodium sulfate, filtered andconcentrated. Purification by preparative HPLC (acetonitrile/water+0.2%ammonium hydroxide) gave the title compound 11.3 mg (29% yield) as awhite solid.

Example 1, Method 48:5-[(5-Methoxypyridin-2-yl)methoxy]-2-(piperazin-1-yl)-1,3-benzoxazole

δ_(H) NMR (500 MHz, DMSO) 8.28 (d, J=2.9 Hz, 1H), 7.47 (d, J=8.6 Hz,1H), 7.42 (dd, J=8.6, 2.9 Hz, 1H), 7.26 (d, J=8.7 Hz, 1H), 6.93 (d,J=2.5 Hz, 1H), 6.64 (dd, J=8.7, 2.6 Hz, 1H), 5.08 (s, 2H), 3.84 (s, 3H),3.53-3.46 (m, 4H), 2.82-2.73 (m, 4H). Tr(MET-uHPLC-AB-101)=1.33 min,(ES⁺) (M+H)⁺ 341.

The following example was prepared using Method 48 described above:

TABLE 49 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

340.38 5-[(5- Methoxypyridin-2- yl)methoxy]-2- (piperazin-1-yl)-1,3-benzoxazole Tr(MET-uHPLC- AB-101) = 1.33 min, (ES⁺) (M + H)⁺ 341Method 49

Step 1, Method 49: Methyl 5-aminopyridine-2-carboxylate

5-Aminopyridine-2-carboxylic acid (2.00 g, 14.5 mmol) was dissolved inanhydrous methanol (20 mL) and cooled to 0° C. Thionyl chloride (3.15mL, 43.4 mmol) was added drop-wise over 5 minutes and the mixtureallowed to warm to room temperature then heated to reflux for 24 hours.The reaction mixture was concentrated, partitioned between ethyl acetate(30 mL) and saturated aqueous sodium bicarbonate solution (30 mL). Themixture was sonicated, the layers separated and the aqueous layerextracted with ethyl acetate (2×15 mL). The combined organic extractswere washed with brine (20 mL), dried over magnesium sulfate, filteredand concentrated to give the title compound 850 mg (39% yield) as anoff-white powder. δ_(H) NMR (500 MHz, DMSO) 7.97 (d, J=2.7 Hz, 1H), 7.74(d, J=8.6 Hz, 1H), 6.91 (dd, J=8.6, 2.7 Hz, 1H), 6.18 (s, 2H), 3.76 (s,3H).

Step 2, Method 49: Methyl5-{[(tert-butoxy)carbonyl]amino}pyridine-2-carboxylate

Methyl 5-aminopyridine-2-carboxylate (850 mg, 5.59 mmol), di-tert-butyldicarbonate (1.34 g, 6.15 mmol) and 4-dimethylaminopyridine (68 mg, 0.56mmol) were suspended in dichloromethane (10 mL) and stirred at roomtemperature for 20 hours. The reaction mixture was concentrated to givea white powder. The powder was suspended in ethyl acetate (20 mL),sonicated, heated to boiling and then filtered. The filtrate was dilutedwith additional ethyl acetate (20 mL) and loaded onto silica.Purification by FCC (silica, 18-100% ethyl acetate in heptane) gave thecrude title compound 862 mg (51% yield) as a white powder which was usedin the next step without further purification. δ_(H) NMR (500 MHz, DMSO)10.01 (s, 1H), 8.71 (d, J=2.3 Hz, 1H), 8.06 (dd, J=8.7, 2.4 Hz, 1H),8.00 (d, J=8.6 Hz, 1H), 3.83 (s, 3H), 1.49 (s, 9H). Tr(METCR1278)=1.64min, (ES⁺) (M+H)⁺ 253, 83%.

Step 3, Method 49: Methyl5-{[(tert-butoxy)carbonyl](methyl)amino}pyridine-2-carboxylate

Methyl 5-{[(tert-butoxy)carbonyl]amino}pyridine-2-carboxylate (406 mg,1.34 mmol) was dissolved in anhydrous N,N-dimethylformamide (5 mL) andcooled to 0° C. Sodium hydride (60% in mineral oil, 136 mg, 3.34 mmol)was added and the mixture stirred for 15 minutes. Iodomethane (100 μL,1.60 mmol) was added and the mixture stirred at room temperature for 18hours. The reaction mixture was quenched by the addition of water (5 mL)and extracted with ethyl acetate (2×15 mL). The combined organicextracts were washed with brine (3×10 mL), dried over magnesium sulfate,filtered and concentrated. Purification by FCC (silica, eluent: 50-75%ethyl acetate in heptane) gave the title compound 180 mg (51% yield) asa yellow oil. δ_(H) NMR (500 MHz, DMSO) 8.70 (d, J=2.5 Hz, 1H), 8.03 (d,J=8.5 Hz, 1H), 7.91 (dd, J=8.5, 2.6 Hz, 1H), 3.87 (s, 3H), 3.27 (s, 3H),1.43 (s, 9H). Tr(METCR1278)=1.68 min, (ES⁺) (M+H)⁺ 267.

Step 4, Method 49: tert-ButylN-[6-(hydroxymethyl)pyridin-3-yl]-N-methylcarbamate

Methyl 5-{[(tert-butoxy)carbonyl](methyl)amino}pyridine-2-carboxylate(170 mg, 0.64 mmol) was dissolved in anhydrous tetrahydrofuran (10 mL)under nitrogen and cooled to 0° C. 1.2 M diisobutylaluminium hydride intoluene (1.06 mL, 1.28 mmol) was added and the mixture stirred for 1.5hours. 1.2 M diisobutylaluminium hydride in toluene (0.13 mL) was addedand the mixture stirred at room temperature for 16 hours. The reactionmixture was quenched with saturated aqueous Rochelle's salt solution (20mL) and extracted with ethyl acetate (2×20 mL). The combined organicextracts were washed with brine (10 mL), dried over magnesium sulfate,filtered and concentrated to give the title compound 120 mg (63% yield)as a colourless gum. δ_(H) NMR (500 MHz, DMSO) 8.41 (d, J=2.5 Hz, 1H),7.71 (dd, J=8.4, 2.6 Hz, 1H), 7.43 (d, J=8.4 Hz, 1H), 5.40 (t, J=5.7 Hz,1H), 4.53 (d, J=5.2 Hz, 2H), 3.19 (s, 3H), 1.39 (s, 9H).Tr(METCR1278)=1.68 min, (ES⁺) (M+H)⁺ 239, 81%.

Step 5, Method 49: tert-ButylN-{6-[(methanesulfonyloxy)methyl]pyridin-3-yl}-N-methylcarbamate

tert-Butyl N-[6-(hydroxymethyl)pyridin-3-yl]-N-methylcarbamate (120 mg,0.4 mmol) was dissolved in dichloromethane (3 mL) under nitrogen andcooled to 0° C. Triethylamine (84 μL, 0.60 mmol) and methanesulfonylchloride (34 μL, 0.44 mmol) were added and the mixture stirred andwarmed to room temperature over 18 hours. The reaction mixture wasdiluted with dichloromethane (5 mL) and washed with water (5 mL) andbrine (5 mL). The organic layer was dried over magnesium sulfate,filtered and concentrated to give the crude title compound 124 mg (42%yield) as an orange oil. The product also contained 47% alkyl chloride.Tr(METCR1278)=1.69 min, (ES⁺) (M+H)⁺ 317, 43% (mesylate).Tr(METCR1278)=1.82 min, (ES⁺) (M+H)⁺ 257/259, 37% (chloride).

Step 6, Method 49: tert-ButylN-methyl-N-[5-({[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)pyridin-2-yl]carbamate

A mixture of tert-butylN-{6-[(methanesulfonyloxy)methyl]pyridin-3-yl}-N-methylcarbamate andtert-butyl N-[6-(chloromethyl)pyridin-3-yl]-N-methylcarbamate (43%+37%,120 mg, 0.34 mmol total alkylating agent) and2-(pyridin-3-yl)-1,3-benzoxazol-5-ol (90 mg, 0.34 mmol, prepared byMethod 14) were dissolved in anhydrous N,N-dimethylformamide (5 mL)under nitrogen and cooled to 0° C. Sodium hydride (60% in mineral oil,41 mg, 1.04 mmol) was added and the mixture stirred and warmed to roomtemperature over 18 hours. The reaction mixture was quenched with water(5 mL) and extracted with ethyl acetate (3×15 mL). The combined ethylacetate extracts were washed with brine (3×10 mL), dried over magnesiumsulfate, filtered and concentrated. Purification by FCC (silica, 12-100%ethyl acetate in heptane) gave the title compound 52 mg (31% yield) as atan powder. δ_(H) NMR (500 MHz, DMSO) 9.33 (d, J=1.6 Hz, 1H), 8.80 (dd,J=4.8, 1.6 Hz, 1H), 8.56 (d, J=2.5 Hz, 1H), 8.51 (dt, J=8.0, 1.9 Hz,1H), 7.78 (dd, J=8.4, 2.6 Hz, 1H), 7.75 (d, J=8.9 Hz, 1H), 7.68-7.62 (m,1H), 7.56 (d, J=8.4 Hz, 1H), 7.50 (d, J=2.5 Hz, 1H), 7.16 (dd, J=8.9,2.6 Hz, 1H), 5.25 (s, 2H), 3.22 (s, 3H), 1.40 (s, 9H).Tr(METCR1278)=2.05 min, (ES⁺) (M+H)⁺ 433, 80%.

Step 7, Method 49:N-Methyl-6-({[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)pyridin-3-amine

tert-ButylN-methyl-N-[5-({[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)pyridin-2-yl]carbamate(52 mg, 0.12 mmol) was dissolved in 4 M hydrogen chloride in 1,4-dioxane(1 mL) and water (0.1 mL). The mixture was stirred at room temperaturefor 1.5 hours and concentrated. Purification by SCX and preparative HPLC(acetonitrile/water+0.1% formic acid) gave the title compound 12 mg (30%yield) as an off-white powder.

Example 1, Method 49:N-Methyl-6-({[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)pyridin-3-amine

δ_(H) NMR (500 MHz, DMSO) 9.32 (d, J=1.5 Hz, 1H), 8.80 (dd, J=4.8, 1.6Hz, 1H), 8.51 (dt, J=8.0, 1.9 Hz, 1H), 7.94 (d, J=2.7 Hz, 1H), 7.72 (d,J=8.9 Hz, 1H), 7.65 (ddd, J=8.0, 4.8, 0.7 Hz, 1H), 7.47 (d, J=2.5 Hz,1H), 7.29 (d, J=8.4 Hz, 1H), 7.10 (dd, J=8.9, 2.5 Hz, 1H), 6.90 (dd,J=8.4, 2.9 Hz, 1H), 5.98 (d, J=5.0 Hz, 1H), 5.06 (s, 2H), 2.70 (d, J=5.0Hz, 3H). Tr(MET-uHPLC-AB-101)=1.67 min, (ES⁺) (M+H)⁺ 333.

The following example was prepared using Method 49 described above:

TABLE 50 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

332.36 N-Methyl-6-({[2- (pyridin-3-yl)-1,3- benzoxazol-5- yl]oxy}methyl)pyridin-3-amine Tr(MET-uHPLC- AB-101) = 1.67 min, (ES⁺) (M + H)⁺ 333Method 50

Step 1, Method 50: 1-(5-Hydroxy-1-benzofuran-2-yl)ethan-1-one

A mixture of 2,5-dihydroxybenzaldehyde (5.0 g, 36.2 mmol),1-chloropropan-2-one (3.6 mL, 43.7 mmol) and potassium carbonate (6.0 g,43.4 mmol) in acetone (100 mL) was heated to reflux for 18 hours. Aftercooling the suspension was diluted with acetone (100 mL) and filteredthrough a plug of celite. The filtrate was concentrated and the residuewas taken up in ethyl acetate (300 mL), washed with water (50 mL) andbrine (50 mL), dried over magnesium sulfate, filtered and absorbed ontoa small amount of silica. Purification by FCC (silica, 0-60% ethylacetate in heptane) gave the title compound 2.99 g (47% yield) as acolourless, crystalline solid. δ_(H) NMR (500 MHz, DMSO) 9.48 (s, 1H),7.80-7.65 (m, 1H), 7.50 (d, J=8.9 Hz, 1H), 7.07 (d, J=2.4 Hz, 1H), 6.98(dd, J=8.9, 2.5 Hz, 1H), 2.52 (s, 3H). Tr(METCR1278)=1.34 min, (ES⁺)(M+H)⁺ 177.

Step 2, Method 50: 1[5-(Methoxymethoxy)-1-benzofuran-2-yl]ethan-1-one

To a solution of 1-(5-hydroxy-1-benzofuran-2-yl)ethan-1-one (2.84 g,16.1 mmol) and chloro(methoxy)methane (3.0 mL, 39.5 mmol) inN,N-dimethylformamide (40 mL) at 0° C. was added sodium hydride (60% inmineral oil, 1.6 g, 40 mmol) in two portions. After 10 minutes theice-bath was removed and the mixture was stirred at room temperature for18 hours. After the addition of methanol (5 mL) stirring was continuedfor 30 minutes before the mixture was added to water (200 mL) and brine(200 mL). The mixture was extracted with ethyl acetate (4×150 mL), thecombined organic layers were washed with brine (100 mL), dried overmagnesium sulfate, filtered and concentrated. The residue was dissolvedin tetrahydrofuran (100 mL) and absorbed onto a small amount of silica.Purification by FCC (silica, 0-50% ethyl acetate in heptane) gave thetitle compound 2.48 g (70% yield) as an off-white solid. δ_(H) NMR (500MHz, DMSO) 7.84-7.79 (m, 1H), 7.64 (d, J=9.0 Hz, 1H), 7.42 (d, J=2.5 Hz,1H), 7.22 (dd, J=9.0, 2.6 Hz, 1H), 5.23 (s, 2H), 3.40 (s, 3H), 2.55 (s,3H). Tr(METCR1278)=1.70 min, (ES⁺) (M+H)⁺ 221.

Step 3, Method 50: Ethyl3-[5-(methoxymethoxy)-1-benzofuran-2-yl]-3-oxopropanoate

To a solution of 1-[5-(methoxymethoxy)-1-benzofuran-2-yl]ethan-1-one(2.45 g, 11.1 mmol) in diethyl carbonate (50 mL, 413 mmol) was addedsodium hydride (60% in mineral oil. 890 mg, 22.3 mmol). After stirringfor 10 minutes at room temperature the mixture was heated to 100° C. for18 hours. The volatiles were removed in vacuo and the residue waspartitioned between ethyl acetate (300 mL), water (100 mL) and aceticacid (2 mL). The organic layer was separated, washed with brine (50 mL),dried over magnesium sulfate, filtered and concentrated. Purification byFCC (silica, 0-20% ethyl acetate in heptane) gave the title compound2.58 g (79% yield) as an off-white solid. δ_(H) NMR (500 MHz, DMSO) 7.91(s, 1H), 7.66 (d, J=9.0 Hz, 1H), 7.44 (d, J=2.5 Hz, 1H), 7.25 (dd,J=9.0, 2.5 Hz, 1H), 5.24 (s, 2H), 4.24-3.96 (m, 4H), 3.40 (d, J=2.2 Hz,3H), 1.18 (t, J=7.1 Hz, 3H). Tr(METCR1278)=1.86 min, (ES⁺) (M+H)⁺ 293.

Step 4, Method 50: Ethyl2-bromo-3-[5-(methoxymethoxy)-1-benzofuran-2-yl]-3-oxopropanoate and2-Bromo-3-(4-bromo-5-hydroxy-1-benzofuran-2-yl)-3-oxopropanoate

To a solution of ethyl3-[5-(methoxymethoxy)-1-benzofuran-2-yl]-3-oxopropanoate (2.5 g, 8.55mmol) in tetrahydrofuran (100 mL) was added phenyltrimethylammoniumtribromide (3.4 g, 9.04 mmol) and the mixture was stirred at roomtemperature for 18 hours. After dilution with ethyl acetate (100 mL) themixture was filtered through celite and the filtrate was concentrated.The residue was taken up in ethyl acetate (300 mL), washed with 10%aqueous sodium thiosulfate (50 mL) and brine (50 mL), dried overmagnesium sulfate, filtered and concentrated to give the title compounds3.20 g (quantitative yield) (3.3/1 mixture by NMR) as a yellow oil.(X═H, major): δ_(H) NMR (500 MHz, DMSO) 9.62 (s, 1H), 8.03-7.92 (m, 1H),7.54 (d, J=9.0 Hz, 1H), 7.12 (d, J=2.4 Hz, 1H), 7.06 (dd, J=9.0, 2.5 Hz,1H), 6.39 (s, 1H), 4.22 (q, J=7.1 Hz, 2H), 1.16 (t, J=7.1 Hz, 3H). (X═H,major): Tr(METCR1278)=1.76 min, (ES⁺) (M+H)⁺ 327/329. (X═Br, minor):Tr(METCR1278)=1.91 min, (ES⁺) (M+H)⁺ 407.

Step 5, Method 50: Ethyl3-(5-hydroxy-1-benzofuran-2-yl)-5H,6H-imidazo[2,1-b][1,3]thiazole-2-carboxylateand Ethyl3-(4-bromo-5-hydroxy-1-benzofuran-2-yl)-5H,6H-imidazo[2,1-b][1,3]thiazole-2-carboxylate

A mixture of crude ethyl2-bromo-3-[5-(methoxymethoxy)-1-benzofuran-2-yl]-3-oxopropanoate and2-bromo-3-(4-bromo-5-hydroxy-1-benzofuran-2-yl)-3-oxopropanoate (ratio:3.3/1, max. 8.55 mmol in total) and imidazolidine-2-thione (880 mg, 8.61mmol) in ethanol (20 mL) and acetic acid (20 mL) was stirred underreflux for 18 hours. The solvent was removed in vacuo and the residuewas triturated with a mixture of ethyl acetate and acetonitrile (20 mL,1/1), filtered and dried under vacuum to give the title compounds 2.58 g(70% yield) (hydrobromide salt, 3/1 mixture by LCMS) as a yellow solid.(X═H, major) Tr(MET-uHPLC-AB-101)=1.52 min, (ES⁺) (M+H)⁺ 331 and (X═Br,minor) Tr(MET-uHPLC-AB-101)=1.81 min, (ES⁺) (M+H)⁺ 409/411.

Step 5, Method 50: Ethyl3-[5-(pyridin-3-ylmethoxy)-1-benzofuran-2-yl]-5H,6H-imidazo[2,1-b][1,3]thiazole-2-carboxylateand Ethyl3-[4-bromo-5-(pyridin-3-ylmethoxy)-1-benzofuran-2-yl]-5H,6H-imidazo[2,1-b][1,3]thiazole-2-carboxylate

To a suspension of ethyl3-(5-hydroxy-1-benzofuran-2-yl)-5H,6H-imidazo[2,1-b][1,3]thiazole-2-carboxylatehydrobromide salt and ethyl3-(4-bromo-5-hydroxy-1-benzofuran-2-yl)-5H,6H-imidazo[2,1-b][1,3]thiazole-2-carboxylatehydrobromide salt (3/1 mixture, 500 mg, 1.15 mmol),3-(bromomethyl)pyridine hydrobromide (480 mg, 1.90 mmol) and potassiumiodide (20 mg, 0.12 mmol) in N,N-dimethylformamide (20 mL) at 0° C. wasadded sodium hydride (60% in mineral oil, 170 mg, 4.26 mmol). The icebath was removed and the mixture was stirred at 60° C. for 90 minutesbefore being partitioned between water (100 mL), brine (100 mL) andethyl acetate (200 mL). The aqueous layer was extracted with ethylacetate (2×100 mL). The combined organic extracts were washed with brine(100 mL), dried over magnesium sulfate, filtered and absorbed onto asmall amount of silica. Purification by FCC (silica, 0-10% methanol indichloromethane) followed by trituration with methanol (3 mL) provided amixture 257 mg (51% yield) of the title compounds (4.3/1 mixture byLCMS) as a yellow solid. (X═H, major) Tr(MET-uHPLC-AB-101)=1.53 min,(ES⁺) (M+H)⁺ 422 and (X═Br, minor) Tr(MET-uHPLC-AB-101)=1.77 min, (ES⁺)(M+H)⁺ 500/502.

Step 6, Method 50:3-[5-(Pyridin-3-ylmethoxy)-1-benzofuran-2-yl]-5H,6H-imidazo[2,1-b][1,3]thiazole-2-carboxamide

A solution of ethyl3-[5-(pyridin-3-ylmethoxy)-1-benzofuran-2-yl]-5H,6H-imidazo[2,1-b][1,3]thiazole-2-carboxylate(81%, 124 mg, 0.24 mmol) in 7 M ammonia in methanol (40 mL) in apressure tube was heated to 80° C. for 24 hours and then stirred at roomtemperature for 3 days. The mixture was added to saturated aqueousammonium chloride solution (300 mL) and then extracted with ethylacetate (4×100 mL). The combined organic extracts were washed with brine(100 mL), dried over magnesium sulfate, filtered and then absorbed ontoa small amount of silica. Purification by FCC (silica, 0-15% methanol indichloromethane) gave the title compound 47 mg (37% yield) as a yellowsolid. δ_(H) NMR (500 MHz, DMSO) 8.69 (d, J=1.8 Hz, 1H), 8.55 (dd,J=4.7, 1.7 Hz, 1H), 7.89 (d, J=7.9 Hz, 1H), 7.58 (d, J=9.0 Hz, 1H), 7.52(s, 1H), 7.44 (dd, J=7.5, 4.7 Hz, 1H), 7.36 (d, J=2.6 Hz, 1H), 7.33 (bs,2H), 7.12 (dd, J=9.0, 2.6 Hz, 1H), 5.22 (s, 2H), 4.16-3.94 (m, 4H).Tr(METCR1278)=1.03 min, (ES⁺) (M+H)⁺ 393, 74%.

Step 7, Method 50:3-[5-(Pyridin-3-ylmethoxy)-1-benzofuran-2-yl]-5H,6H-imidazo[2,1-b][1,3]thiazole-2-carbonitrile

To a solution of3-[5-(pyridin-3-ylmethoxy)-1-benzofuran-2-yl]-5H,6H-imidazo[2,1-b][1,3]thiazole-2-carboxamide(74%, 44 mg, 0.083 mmol) and pyridine (0.02 mL, 0.248 mmol) intetrahydrofuran (10 mL) at 0° C. was added trifluoroacetic anhydride (50μL, 0.35 mmol). After stirring for 10 minutes the mixture was added tosaturated aqueous sodium bicarbonate solution and extracted with ethylacetate (3×50 mL). The combined organic extracts were washed with brine(50 mL), dried over magnesium sulfate, filtered and concentrated.Purification by preparative HPLC (acetonitrile/water+0.2% ammoniumhydroxide) gave the title compound 12 mg (39% yield) as a yellow solid.

Example 1, Method 50:3-[5-(Pyridin-3-ylmethoxy)-1-benzofuran-2-yl]-5H,6H-imidazo[2,1-b][1,3]thiazole-2-carbonitrile

δ_(H) NMR (500 MHz, DMSO) 8.71 (d, J=1.9 Hz, 1H), 8.56 (dd, J=4.8, 1.5Hz, 1H), 7.96-7.85 (m, 1H), 7.70-7.57 (m, 2H), 7.51-7.37 (m, 2H), 7.20(dd, J=9.2, 2.6 Hz, 1H), 5.22 (s, 2H), 4.34-4.18 (m, J=5.1 Hz, 4H).Tr(MET-uHPLC-AB-101)=1.22 min, (ES⁺) (M+H)⁺ 375.

The following example was prepared using Method 50 described above:

TABLE 51 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

374.42 3-[5-(Pyridin-3- ylmethoxy)-1- benzofuran-2-yl]- 5H,6H-imidazo[2,1-b] [1,3]thiazole-2- carbonitrile Tr(MET-uHPLC- AB-101) =1.22 min, (ES⁺) (M + H)⁺ 375Method 51

Step 1, Method 51:5-N-{2-Hydroxy-5-[(5-methoxypyridin-2-yl)methoxy]phenyl}-2-N-methylpyridine-2,5-dicarboxamide

To a solution of 2-amino-4-[(5-methoxypyridin-2-yl)methoxy]phenol (100mg, 0.41 mmol, prepared by Method 33) in pyridine (2 mL) and6-(methylcarbamoyl)pyridine-3-carboxylic acid (80 mg, 0.45 mmol,prepared as described in PCT Int. Appl 2006003378) in pyridine (2 mL)was added N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride(101.2 mg, 0.53 mmol) and the mixture was stirred at room temperaturefor 18 hours. The solvent was removed in vacuo and the residue was takenup in ethyl acetate (50 mL), washed with water (2×10 mL) and dried oversodium sulfate. Filtration and concentration gave the title compound 164mg (89% yield, 72% purity) as a yellow powder. The crude product wastaken directly into the next step.

Step 2, Method 51:5-{5-[(5-Methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-N-methylpyridine-2-carboxamide

Crude5-N-{2-hydroxy-5-[(5-methoxypyridin-2-yl)methoxy]phenyl}-2-N-methylpyridine-2,5-dicarboxamide(164 mg, 2.91 mmol, 72% purity) was suspended in acetic acid (3 mL) andheated in a microwave at 200° C. for 40 minutes. After cooling thevolatiles were removed in vacuo and the residue was distributed betweenethyl acetate (2 mL) and saturated aqueous sodium bicarbonate solution(10 mL). The mixture was filtered, the solid was washed with warmmethanol (30 mL) and the solution concentrated. Purification by FCC(silica, 12-100% ethyl acetate in heptane) gave the title compound 9 mg(8% yield) as a white powder.

Example 1, Method 51:5-{5-[(5-Methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-N-methylpyridine-2-carboxamide

δ_(H) NMR (500 MHz, DMSO) 9.34 (d, J=2.0 Hz, 1H), 8.97 (q, J=4.8 Hz,1H), 8.68 (dd, J=8.2, 2.1 Hz, 1H), 8.31 (d, J=2.9 Hz, 1H), 8.23 (d,J=8.2 Hz, 1H), 7.77 (d, J=8.9 Hz, 1H), 7.53 (d, J=8.6 Hz, 1H), 7.51 (d,J=2.5 Hz, 1H), 7.44 (dd, J=8.6, 3.0 Hz, 1H), 7.17 (dd, J=8.9, 2.5 Hz,1H), 5.20 (s, 2H), 3.84 (s, 3H), 2.85 (d, J=4.8 Hz, 3H).Tr(MET-uHPLC-AB-101)=2.71 min, (ES⁺) (M+H)⁺ 391.

The following example was prepared using Method 51 described above:

TABLE 52 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

390.39 5-{5-[(5- Methoxypyridin-2- yl)methoxy]-1,3- benzoxazol-2-yl}-N-methylpyridine- 2-carboxamide Tr(MET-uHPLC- AB-101) = 2.71 min, (ES⁺)(M + H)⁺ 391Method 52

Step 1, Method 52:N-{2-Hydroxy-5-[(5-methoxypyridin-2-yl)methoxy]phenyl}-1-methyl-1H-imidazole-4-carboxamide

To a solution of 2-amino-4-[(5-methoxypyridin-2-yl)methoxy]phenol (50%,300 mg, 0.61 mmol, prepared by Method 33) and1-methyl-1H-imidazole-4-carboxylic acid (85 mg, 0.67 mmol) in pyridine(3 mL) was added 1-(3-(dimethylamino)-propyl)-3-ethylcarbodiimidehydrochloride (150 mg, 0.78 mmol) and the mixture was stirred at roomtemperature for 18 hours. The solvent was removed in vacuo and theresidue was taken up in ethyl acetate (200 mL), washed with water (50mL) and brine (50 mL), dried over magnesium sulfate, filtered andconcentrated. The residue was dissolved in methanol (50 mL) and stirredunder reflux for 2 days. After cooling the crude product waspre-absorbed onto a small amount of silica and then purified by FCC(silica, 0-10% methanol in ethyl acetate) to give the title compound 25mg (12% yield) as off-white solid. Tr(METCR1278)=1.35 min, (ES⁺) (M+H)⁺355.

Step 2, Method 52:5-[(5-Methoxypyridin-2-yl)methoxy]-2-(1-methyl-1H-imidazol-4-yl)-1,3-benzoxazoleformate salt

N-{2-Hydroxy-5-[(5-methoxypyridin-2-yl)methoxy]phenyl}-1-methyl-1H-imidazole-4-carboxamide(25 mg, 0.07 mmol) was suspended in acetic acid (1 mL) and heated in amicrowave at 200° C. for 40 minutes. After cooling the volatiles wereremoved in vacuo and the residue was partitioned between ethyl acetate(100 mL) and saturated aqueous sodium bicarbonate (50 mL). The organiclayer was washed with brine (50 mL), dried over magnesium sulfate,filtered and concentrated. Purification by preparative HPLC(acetonitrile/water+0.1% formic acid) gave the title compound 8.6 mg(32% yield) as off-white solid.

Step 2, Method 52:5-[(5-Methoxypyridin-2-yl)methoxy]-2-(1-methyl-1H-imidazol-4-yl)-1,3-benzoxazoleformate salt

δ_(H) NMR (500 MHz, DMSO) 8.33 (s, 1H), 8.30 (d, J=2.9 Hz, 1H), 8.04 (d,J=1.0 Hz, 1H), 7.83 (s, 1H), 7.60 (d, J=8.8 Hz, 1H), 7.51 (d, J=8.6 Hz,1H), 7.43 (dd, J=8.6, 3.0 Hz, 1H), 7.33 (d, J=2.5 Hz, 1H), 7.00 (dd,J=8.8, 2.5 Hz, 1H), 5.15 (s, 2H), 3.83 (s, 3H), 3.76 (s, 3H).Tr(MET-uHPLC-AB-101)=1.96 min, (ES⁺) (M+H)⁺ 337.

The following example was prepared using Method 52 described above:

TABLE 53 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

336.34 5-[(5- Methoxypyridin-2- yl)methoxy]-2-(1- methyl-1H-imidazol-4-yl)-1,3- benzoxazole Tr(MET-uHPLC- AB-101) = 1.96 min, (ES⁺)(M + H)⁺ 337Method 53

Step 1, Method 53: 2-(Pyridin-3-yl)-1,3-benzoxazole-5-carbaldehyde

To a stirred solution of [2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]methanol(149 mg, 0.66 mmol, prepared by Method 23) in tetrahydrofuran (10 mL)under nitrogen, was added1,1,1-triacetoxy-1,1-dihydro-1,2-benziodoxol-3(1H)-one (307 mg, 0.72mmol). The mixture was stirred at room temperature for 1.5 hours. Themixture was filtered and concentrated. The residue was triturated indichloromethane-methanol (9:1, 5 mL) and filtered. The filtrate wasconcentrated and purified by FCC (silica, 12-100% ethyl acetate inheptane) to give the title compound 152 mg (100% yield) as a whitepowder. δ_(H) NMR (500 MHz, DMSO) 10.13 (s, 1H), 9.39 (s, 1H), 8.85 (d,J=4.8 Hz, 1H), 8.59 (d, J=8.0 Hz, 1H), 8.41 (s, 1H), 8.06 (s, 2H), 7.69(dd, J=8.0, 4.9 Hz, 1H). Tr(METCR1278)=1.57 min, (ES⁺) (M+H)⁺ 225.

Step 1, Method 53:5-Methoxy-N-{[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]methyl}pyridin-2-amine

A solution of 2-(pyridin-3-yl)-1,3-benzoxazole-5-carbaldehyde (50 mg,0.22 mmol) and 5-methoxypyridin-2-amine (30 mg, 0.25 mmol) in toluene (5mL) was treated with diethyl2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate (68 mg, 0.27 mmol),thiourea (3 mg, 0.04 mmol) and molecular sieves (4 Å, 223 mg) and themixture was stirred at 70° C. under nitrogen for 2 days.2,6-Dimethyl-1,4-dihydropyridine-3,5-dicarboxylate (40 mg, 0.16 mmol)was added and the mixture stirred at 70° C. overnight. After filtrationthrough celite, the filtrate was concentrated and the residue purifiedby FCC (silica, 20-100% ethyl acetate in heptane) to give the titlecompound 72 mg (97% yield) as an off white powder.

Example, 1 Method 53:5-Methoxy-N-{[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]methyl}pyridin-2-amine

δ_(H) NMR (500 MHz, DMSO) 9.34 (d, J=1.9 Hz, 1H), 8.80 (dd, J=4.8, 1.5Hz, 1H), 8.52 (dt, J=8.0, 1.9 Hz, 1H), 7.77-7.70 (m, 3H), 7.65 (dd,J=8.0, 4.8 Hz, 1H), 7.44 (dd, J=8.4, 1.3 Hz, 1H), 7.14 (dd, J=9.0, 3.0Hz, 1H), 6.79 (t, J=6.1 Hz, 1H), 6.52 (d, J=9.0 Hz, 1H), 4.55 (d, J=6.1Hz, 2H), 3.67 (s, 3H). Tr(MET-uHPLC-AB-101)=1.49 min, (ES⁺) (M+H)⁺ 333.

The following example was prepared using Method 53 described above:

TABLE 54 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

332.36 5-Methoxy-N-{[2- (pyridin-3-yl)-1,3- benzoxazol-5-yl]methyl}pyridin- 2-amine Tr(MET-uHPLC- AB-101) = 1.49 min, (ES⁺) (M +H)⁺ 333Method 54

Step 1, Method 54:5-({5-[2-(Morpholin-4-yl)ethoxy]pyridin-2-yl}methoxy)-2-(pyridin-3-yl)-1,3-benzoxazole

6-({[2-(Pyridin-3-yl)-1,3-benzoxazol-5-yl]oxy}methyl)pyridin-3-ol (50%,59 mg, 0.09 mmol prepared by Method 27), 4-(2-chloroethyl)morpholinehydrochloride (20 mg, 0.11 mmol) and potassium iodide (15 mg, 0.09 mmol)were dissolved in anhydrous N,N-dimethylformamide (1 mL), sodium hydride(7 mg, 0.28 mmol) was added and the reaction was stirred at roomtemperature for 16 hours. The reaction was heated to 60° C. for 4 hours.The reaction mixture was cooled to room temperature and partitionedbetween ethyl acetate and water (1:1, 10 mL). The aqueous was extractedwith ethyl acetate (2×10 mL). The combined organics were washed withwater (2×1 mL), brine (2 mL), dried over sodium sulfate, filtered, andconcentrated. Purification by preparative HPLC (acetonitrile/water+0.2%ammonium hydroxide) gave the title compound 2 mg (5% yield) as a whitesolid.

Example 1, Method 54:5-({5-[2-(Morpholin-4-yl)ethoxy]pyridin-2-yl}methoxy)-2-(pyridin-3-yl)-1,3-benzoxazole

δ_(H) NMR (500 MHz, DMSO) 9.32 (s, 1H), 8.80 (d, J=3.8 Hz, 1H), 8.50(dt, J=8.0, 1.9 Hz, 1H), 8.30 (d, J=2.8 Hz, 1H), 7.73 (d, J=8.9 Hz, 1H),7.65 (dd, J=8.0, 4.8 Hz, 1H), 7.59-7.33 (m, 3H), 7.13 (dd, J=8.9, 2.5Hz, 1H), 5.18 (s, 2H), 4.17 (t, J=5.7 Hz, 2H), 3.64-3.45 (m, 4H), 2.70(t, J=5.7 Hz, 2H), 2.49-2.41 (m, 4H). Tr(MET-uHPLC-AB-101)=1.59 min,(ES⁺) (M+H)⁺ 433.

The following example was prepared using Method 54 described above:

TABLE 55 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

432.47 5-({5-[2- (Morpholin-4- yl)ethoxy]pyridin- 2-yl}methoxy)-2-(pyridin-3-yl)-1,3- benzoxazole Tr(MET-uHPLC- AB-101) = 1.59 min, (ES⁺)(M + H)⁺ 433Method 55

Step 1, Method 55: (5-Methoxy-1-benzofuran-2-yl)boronic acid

2.5 M n-butyllithium in hexanes (2.8 mL, 7.00 mmol) was added slowly toa solution of 5-methoxy-1-benzofuran (1.0 g, 6.75 mmol) in drytetrahydrofuran (15 mL) at −78° C. under a nitrogen atmosphere. After 1hour stirring at −78° C., triisopropylborate (3.12 mL, 13.5 mmol) wasadded drop-wise and the mixture stirred for 30 minutes at −78° C. Thedry ice bath was removed, 2 M aqueous hydrochloric acid (20 mL) wasadded and the mixture warmed to room temperature whilst stirringovernight. The reaction mixture was poured into water (25 mL) andextracted with diethyl ether (3×20 mL). The combined organics werewashed with brine (20 mL), dried over magnesium sulfate, filtered andconcentrated under reduced pressure. Dichloromethane (20 mL) was addedand the mixture sonicated for 10 minutes. The minimum amount of methanol(ca. 1 mL) was added to fully dissolve the solids and the solutionsonicated for 10 minutes. Heptane (20 mL) was added and the precipitatedsolids collected by vacuum filtration and allowed to dry under vacuumfor 2 hours to give the title compound 476 mg (37% yield) as a whitesolid. δ_(H) NMR (500 MHz, DMSO) 8.53 (s, 2H), 7.46 (d, J=8.94 Hz, 1H),7.39 (s, 1H), 7.19 (d, J=2.51 Hz, 1H), 6.93 (dd, J=2.60, 8.92 Hz, 1H),3.78 (s, 3H).

Step 2, Method 55: 2-Bromo-6-(5-methoxy-1-benzofuran-2-yl)benzonitrile

A mixture of (5-methoxy-1-benzofuran-2-yl)boronic acid (156 mg, 0.813mmol), 2-bromo-6-iodobenzonitrile (250 mg, 0.81 mmol) and 2 M sodiumcarbonate (0.82 mL, 1.64 mmol) in N,N-dimethylformamide (10 mL) wassonicated under a stream of nitrogen for 20 minutes.[1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II) complex withdichloromethane (50 mg, 0.14 mmol) was added and the mixture was stirredat 70° C. for 2 hours. After cooling the mixture was added to water (100mL) and brine (100 mL). The mixture was extracted with ethyl acetate(3×100 mL), the combined extracts were washed with brine (50 mL), driedover magnesium sulfate, filtered and concentrated. Purification by FCC(silica, 0-50% ethyl acetate in heptane) gave the title compound 168 mg(37% yield, 82% pure by LCMS) as an off-white solid, which was taken ondirectly into the next step. A sample was purified by preparative HPLC(acetonitrile/water+0.1% formic acid) δ_(H) NMR (500 MHz, DMSO) 8.09 (d,J=8.0 Hz, 1H), 7.93 (d, J=8.0 Hz, 1H), 7.76 (t, J=8.1 Hz, 1H), 7.70 (s,1H), 7.58 (d, J=9.0 Hz, 1H), 7.32 (d, J=2.6 Hz, 1H), 7.02 (dd, J=9.0,2.6 Hz, 1H), 3.81 (s, 3H). Tr(MET-uHPLC-AB-101)=5.45 min, (ES⁺) (M+H)⁺328/330.

Step 3, Method 55: 2-Bromo-6-(5-hydroxy-1-benzofuran-2-yl)benzonitrile

1 M Boron tribromide in dichloromethane (2.0 mL, 2.0 mmol) was addeddrop-wise over 5 minutes to a stirred solution of2-bromo-6-(5-methoxy-1-benzofuran-2-yl)benzonitrile (0.13 g, 0.39 mmol),in dichloromethane (15 mL) at room temperature and the resultingsolution was stirred for 1 hour. The reaction was quenched by theaddition of methanol (5 mL). The solvents were evaporated to give thetitle compound 0.12 g (77% yield) as a beige solid. δ_(H) NMR (500 MHz,chloroform) 8.05 (d, J=8.12 Hz, 1H), 7.70 (s, 1H), 7.66 (d, J=7.23 Hz,1H), 7.53 (t, J=8.08 Hz, 1H), 7.40 (d, J=8.80 Hz, 1H), 7.06 (d, J=2.54Hz, 1H), 6.91 (dd, J=2.57, 8.81 Hz, 1H).

Step 4, Method 55:2-Bromo-6-{5-[(5-methoxypyridin-2-yl)methoxy]-1-benzofuran-2-yl}benzonitrile

To a stirred solution of2-bromo-6-(5-hydroxy-1-benzofuran-2-yl)benzonitrile (0.12 g, 0.38 mmol)and 2-(chloromethyl)-5-methoxypyridine hydrochloride (0.07 g, 0.38 mmol)in N,N-dimethylformamide (8 mL) under nitrogen, was added sodium hydride(60% in mineral oil, 0.03 g, 0.84 mmol) portion-wise at 0° C. Themixture was allowed to warm to room temperature and stirred for 48hours. The mixture was quenched with water (4 mL) and the solventsremoved in vacuo. The residue was partitioned between ethyl acetate (150mL) and water (150 mL) and the aqueous layer was extracted with ethylacetate (3×100 mL). The combined organic extracts were washed with brine(2×20 mL), dried over magnesium sulfate, filtered and concentrated.Purification by preparative HPLC (acetonitrile/water+0.2% ammoniumhydroxide) gave the title compound 29 mg (17% yield) as a white,crystalline solid.

Example 1, Method 55:2-Bromo-6-{5-[(5-methoxypyridin-2-yl)methoxy]-1-benzofuran-2-yl}benzonitrile

δ_(H) NMR (500 MHz, DMSO) 8.31 (d, J=2.9 Hz, 1H), 8.10 (d, J=8.0 Hz,1H), 7.94 (d, J=8.1 Hz, 1H), 7.77 (t, J=8.1 Hz, 1H), 7.70 (s, 1H), 7.61(d, J=9.0 Hz, 1H), 7.52 (d, J=8.6 Hz, 1H), 7.48-7.36 (m, 2H), 7.12 (dd,J=9.0, 2.6 Hz, 1H), 5.16 (s, 2H), 3.84 (s, 3H).Tr(MET-uHPLC-AB-101)=4.12 min, (ES⁺) (M+H)⁺ 437/439.

The following example was prepared using Method 55 described above:

TABLE 56 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

435.27 2-Bromo-6-{5-[(5- methoxypyridin-2- yl)methoxy]-1- benzofuran-2-yl}benzonitrile Tr(MET-uHPLC- AB-101) = 4.12 min, (ES⁺) (M + H)⁺ 437/439Method 56

Step 1, Method 56:4-(5-{5H,6H-Imidazo[2,1-b][1,3]thiazol-3-ylmethoxy}-1-benzofuran-2-yl)pyridine-3-carbonitrilehydrochloride

To a mixture of 4-(5-hydroxy-1-benzofuran-2-yl)pyridine-3-carbonitrile(150 mg, 0.63 mmol, prepared by Method 9),3-(chloromethyl)-5H,6H-imidazo[2,1-b][1,3]thiazole (170 mg, 0.97 mmol)and potassium iodide (10 mg, 0.06 mmol) in N,N-dimethylformamide (10 mL)was added sodium hydride (60% in mineral oil, 90 mg, 2.25 mmol). Themixture was stirred for 3 hours at room temperature then added to amixture of water (150 mL) and brine (150 mL) and extracted with ethylacetate (4×100 mL). The combined organic extracts were washed with brine(100 mL), dried over magnesium sulfate, filtered and concentrated. Theresidue was taken up in methanol (30 mL) and 1 M hydrochloric acid (3mL) was added before the volatiles were removed in vacuo. The residuewas triturated with DMSO:water (3 mL, 4:1 mixture) to give the titlecompound 19 mg (7% yield) as an off-white, crystalline solid.

Example 1, Method 56:4-(5-{5H,6H-Imidazo[2,1-b][1,3]thiazol-3-ylmethoxy}-1-benzofuran-2-yl)pyridine-3-carbonitrilehydrochloride

δ_(H) NMR (500 MHz, DMSO) 9.68 (s, 1H), 9.13 (s, 1H), 8.94 (d, J=5.4 Hz,1H), 8.08 (d, J=5.4 Hz, 1H), 7.96 (s, 1H), 7.70 (d, J=9.0 Hz, 1H), 7.55(d, J=2.6 Hz, 1H), 7.21 (dd, J=9.0, 2.6 Hz, 1H), 7.06 (s, 1H), 5.17 (s,2H), 4.48 (dd, J=11.2, 8.2 Hz, 2H), 4.31 (dd, J=11.2, 8.2 Hz, 2H).Tr(METCR1416)=2.96 min, (ES⁺) (M+H)⁺ 375.

The following example was prepared using Method 56 described above:

TABLE 57 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

374.42 4-(5-{5H,6H- Imidazo[2,1-b] [1,3]thiazol-3- ylmethoxy}-1-benzofuran-2- yl)pyridine-3- carbonitrile Tr(METCR1416) = 2.96 min,(ES⁺) (M + H)⁺ 375Method 57

Step 1, Method 57:2-(3-Bromopyridin-4-yl)-6-methoxy-1,3-benzothiazole

2-Amino-5-methoxybenzene-1-thiol (80%, 1 g, 5.15 mmol, described in J.Med. Chem., (2003) 46, 2740), 3-bromopyridine-4-carbaldehyde (0.98 g,5.26 mmol) and sodium metabisulfite (1 g, 5.26 mmol) were dissolved inanhydrous dimethylsulfoxide (5 mL). The reaction mixture was stirred at120° C. for 2 hours. The mixture was cooled to room temperature andwater (100 mL) was added. The resulting black precipitate was filteredand washed with water. The precipitate was dissolved in dichloromethane.The suspension was passed through a pad of silica. The pad was washedwith dichloromethane to give the title compound 1.123 g (68% yield) as apurple solid. δ_(H) NMR (500 MHz, DMSO) 8.99 (s, 1H), 8.71 (d, J=5.0 Hz,1H), 8.13 (d, J=5.0 Hz, 1H), 8.07 (d, J=9.0 Hz, 1H), 7.83 (d, J=2.0 Hz,1H), 7.23 (dd, J=8.9, 2.2 Hz, 1H), 3.88 (s, 3H).Tr(MET-uHPLC-AB-101)=3.57 min, (ES⁺) (M+H)⁺ 321/323.

Step 2, Method 57: 2-(3-Bromopyridin-4-yl)-1,3-benzothiazol-6-ol

To a suspension of 2-(3-bromopyridin-4-yl)-6-methoxy-1,3-benzothiazole(200 mg, 0.62 mmol) in dichloromethane (6 mL) was added boron tribromide(1 M in dichloromethane, 2.80 mL, 2.80 mmol) and the mixture was stirredat room temperature for 24 hours. The reaction was quenched with water(10 mL), neutralized with solid sodium hydrogen carbonate (6 mmol) andextracted with a dichloromethane:ethanol 4:1 solution (3×20 mL). Theorganic layers were combined, washed with water (20 mL), dried oversodium sulfate, filtered and concentrated. The residue was purified byFCC (silica, 0-100% ethyl acetate in toluene, then 5-20% methanol inethyl acetate, then 0-30% methanol in dichloromethane, thenacetonitrile). The silica of the column was washed with adichloromethane:isopropanol 4:1 solution (3×100 mL). The suspension wasfiltered. The filtrate was combined with the fractions containing thetitle compound and concentrated. The residue was dissolved in hotmethanol and filtered. The filtrate was allowed to stand at roomtemperature for 18 hours. The precipitate was filtered. 50 mg weresonicated in 2 M aqueous sodium hydroxide (5 mL). The mixture was washedwith ethyl acetate (5 mL). The aqueous phase was treated with a 2 Mhydrochloric solution up to pH 7 and extracted with ethyl acetate (3×10mL). The organic layers were combined, dried over sodium sulfate,filtered and concentrated. The residue was triturated in hot ethylacetate and filtered to give the title compound 5.4 mg (3% yield) as anoff white solid. δ_(H) NMR (500 MHz, DMSO) 8.97 (s, 1H), 8.69 (d, J=5.0Hz, 1H), 8.11 (d, J=5.0 Hz, 1H), 7.98 (d, J=8.8 Hz, 1H), 7.50 (d, J=2.2Hz, 1H), 7.08 (dd, J=8.9, 2.3 Hz, 1H). Tr(MET-uHPLC-AB-101)=2.67 min,(ES⁺) (M+H)⁺ 307/309.

Step 3, Method 57:2-(3-Bromopyridin-4-yl)-6-[2-(morpholin-4-yl)ethoxy]-1,3-benzothiazole

2-(3-Bromopyridin-4-yl)-1,3-benzothiazol-6-ol (35 mg, 0.11 mmol),4-(2-chloroethyl)morpholine hydrochloride (23 mg, 0.13 mmol) andpotassium carbonate (55 mg, 0.4 mmol) were stirred at room temperaturein N,N-dimethylformamide (1 mL) for 16 hours. The mixture was heated to80° C. for 2 hours. The mixture was cooled to room temperature and water(10 mL) was added. The mixture was extracted with ethyl acetate (3×5mL). The organic layers were combined, washed with brine (5 mL) andevaporated in vacuo. Purification by FCC (silica, 0-50% ethyl acetate indichloromethane then 5% methanol in dichloromethane) gave the titlecompound 36 mg (75% yield) as a white solid.

Example 1, Method 57:2-(3-Bromopyridin-4-yl)-6-[2-(morpholin-4-yl)ethoxy]-1,3-benzothiazole

δ_(H) NMR (500 MHz, chloroform) 8.91 (s, 1H), 8.63 (d, J=5.1 Hz, 1H),8.12 (d, J=5.1 Hz, 1H), 8.04 (d, J=9.0 Hz, 1H), 7.42 (d, J=2.3 Hz, 1H),7.18 (dd, J=9.0, 2.5 Hz, 1H), 4.26 (s, 2H), 3.79 (s, 4H), 2.92 (s, 2H),2.67 (s, 4H). Tr(MET-uHPLC-AB-101)=1.59 min, (ES⁺) (M+H)⁺ 420/422.

The following example was prepared using Method 57 described above:

TABLE 58 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

420.32 2-(3- Bromopyridin-4- yl)-6-[2- (morpholin-4- yl)ethoxy]-1,3-benzothiazole Tr(MET-uHPLC- AB-101) = 1.59 min, (ES+) (M + H)+ 420/422Method 58

Step 1, Method 56: tert-Butyl4-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]piperazine-1-carboxylate

A sealed tube was charged with 5-bromo-2-(pyridin-3-yl)-1,3-benzoxazole(200 mg, 0.73 mmol), tert-butyl piperazine-1-carboxylate (162 mg, 0.87mmol), caesium carbonate (568 mg, 1.74 mmol),[2′,6′-bis(propan-2-yloxy)biphenyl-2-yl](dicyclohexyl)phosphane (17 mg,0.04 mmol) and tetrahydrofuran (5 mL). The reaction mixture was degassedby bubbling with nitrogen for 20 minutes. Palladium(II) acetate (8 mg,0.04 mmol) was added and the reaction mixture was stirred overnight at70° C. The reaction mixture was cooled to room temperature andpartitioned between ethyl acetate (15 mL) and water (15 mL). The aqueouslayer was separated and extracted with ethyl acetate (2×15 mL). Thecombined organic extracts were dried over sodium sulfate, filtered andconcentrated. Purification by FCC (silica, 10-100% ethyl acetate inheptane) gave the title compound 235 mg (85% yield) as a yellow powder.

Example 1, Method 58: tert-butyl4-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]piperazine-1-carboxylate

δ_(H) NMR (500 MHz, DMSO) 9.32 (d, J=2.1 Hz, 1H), 8.79 (dd, J=4.8, 1.6Hz, 1H), 8.50 (dt, J=8.0, 1.9 Hz, 1H), 7.68 (d, J=9.0 Hz, 1H), 7.64 (dd,J=8.0, 4.8 Hz, 1H), 7.35 (d, J=2.4 Hz, 1H), 7.17 (dd, J=9.0, 2.4 Hz,1H), 3.49 (d, J=4.9 Hz, 4H), 3.16-3.09 (m, 4H), 1.43 (s, 9H).Tr(MET-uHPLC-AB-101)=3.5 min, (ES⁺) (M+H)⁺ 381.

The following example was prepared using Method 58 described above:

TABLE 59 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

380.44 tert-Butyl 4-[2- (pyridin-3-yl)-1,3- benzoxazol-5-yl]piperazine-1- carboxylate Tr(MET-uHPLC- AB-101) = 3.5 min, (ES⁺) (M +H)⁺ 381Method 59

Step 1, Method 59: 5-[2-(Pyridin-3-yl)-1,3-benzoxazol-5-yl]pyrazin-2-ol

5-(5-Methoxypyrazin-2-yl)-2-(pyridin-3-yl)-1,3-benzoxazole (344 mg, 0.96mmol, prepared using Method 8) and sodium iodide (216 mg, 1.44 mmol)were suspended in acetonitrile (30 mL), chloro(trimethyl)silane (182 μl,1.44 mmol) was added and the reaction was sealed and stirred at roomtemperature for 60 hours. The reaction was heated to 70° C. for 8 hours.The reaction was stirred at room temperature for 15 hours. The reactionmixture was filtered through paper and the precipitate was washed withwater (10 mL) and diethyl ether (2×10 mL). The solid was dried in vacuoto give the title compound, 220 mg (78% yield) as a brown solid.

Example 1, Method 59:5-[2-(Pyridin-3-yl)-1,3-benzoxazol-5-yl]pyrazin-2-ol

δ_(H) NMR (500 MHz, DMSO) 12.67 (br. s., 1H), 9.38 (d, J=2.1 Hz, 1H),8.83 (dd, J=4.8, 1.6 Hz, 1H), 8.56 (dt, J=8.0, 1.9 Hz, 1H), 8.38-8.24(m, 1H), 8.20 (br. s., 1H), 8.16 (d, J=1.1 Hz, 1H), 8.02 (dd, J=8.6, 1.5Hz, 1H), 7.88 (d, J=8.6 Hz, 1H), 7.68 (dd, J=8.0, 4.8 Hz, 1H).Tr(MET-uHPLC-AB-101)=1.88 min, (ES⁺) (M+H)⁺ 291.

The following example was prepared using Method 59 described above:

TABLE 60 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

290.28 5-[2-(Pyridin-3-yl)- 1,3-benzoxazol-5- yl]pyrazin-2-olTr(MET-uHPLC- AB-101) = 1.88 min, (ES⁺) (M + H)⁺ 291Method 60

Step 1, Method 60: 2-Chloro-5-(2-methoxyethoxy)pyrimidine

2-Chloropyrimidin-5-ol (200 mg, 1.53 mmol), 1-bromo-2-methoxyethane(0.158 mL, 1.69 mmol) and potassium carbonate (423.5 mg, 3.06 mmol) weresuspended in anhydrous N,N-dimethylformamide (5 mL) and heated to 50° C.in a nitrogen atmosphere for 16 hours. The solvents were removed invacuo and the residue was partitioned between ethyl acetate (50 mL) andwater (30 mL), the aqueous was extracted with ethyl acetate (2×30 mL)and the combined organics washed with brine (20 mL), dried overanhydrous sodium sulfate, filtered and concentrated to give the titlecompound 244 mg (yield 85%) as off-white translucent crystals. δ_(H) NMR(500 MHz, DMSO) 8.55 (s, 2H), 4.37-4.21 (m, 2H), 3.78-3.59 (m, 2H), 3.30(s, 3H). Tr(METCR1278)=1.36 min, (ES⁺) (M+Na)⁺ 189.

Step 2, Method 60:5-[5-(2-Methoxyethoxy)pyrimidin-2-yl]-2-(pyridin-3-yl)-1,3-benzoxazole

2-(Pyridin-3-yl)-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3-benzoxazole(205 mg, 0.57 mmol, prepared using Method 8),2-chloro-5-(2-methoxyethoxy)pyrimidine (119 mg, 0.63 mmol) and 2 Msodium carbonate (0.57 mL) were suspended in anhydrous 1,4-dioxane (4mL) and sonicated under a flow of nitrogen for 5 minutes.Tetrakis(triphenylphosphine)palladium(0) (33 mg, 0.03 mmol) was addedand the reaction mixture heated to 110° C. for 6 hours. The reactionmixture was cooled to room temperature and concentrated in vacuo. Theresidue was partitioned between ethyl acetate (50 mL) and water (50 mL).The aqueous was extracted with ethyl acetate (2×50 mL), the combinedorganics washed with brine solution (20 mL), dried over anhydrous sodiumsulfate, filtered and concentrated. The residue was purified by FCC(silica, 20% tetrahydrofuran in dichloromethane) to give the titlecompound 33.5 mg (yield 17%) as a white solid.

Example 1, Method 60:5-[5-(2-Methoxyethoxy)pyrimidin-2-yl]-2-(pyridin-3-yl)-1,3-benzoxazole

δ_(H) NMR (500 MHz, DMSO) 9.39 (d, J=2.1 Hz, 1H), 8.83 (dd, J=4.8, 1.6Hz, 1H), 8.71 (s, 2H), 8.68 (d, J=1.6 Hz, 1H), 8.64-8.52 (m, 1H), 8.47(dd, J=8.6, 1.7 Hz, 1H), 7.94 (d, J=8.6 Hz, 1H), 7.68 (dd, J=7.9, 4.9Hz, 1H), 4.69-4.11 (m, 2H), 3.85-3.58 (m, 2H), 3.33 (s, 3H).Tr(MET-uHPLC-AB-101)=2.85 min, (ES⁺) (M+H)⁺ 349.

The following example was prepared using Method 60 described above:

TABLE 61 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

348.36 5-[5-(2- Methoxyethoxy) pyrimidin-2-yl]- 2-(pyridin-3-yl)- 1,3-benzoxazole Tr(MET-uHPLC- AB-101) = 2.85 min, (ES⁺) (M + H)⁺ 349Method 61

Step 1, Method 61:6-Fluoro-N-{2-hydroxy-5-[(5-methoxypyridin-2-yl)methoxy]phenyl}pyridine-3-carboxamide

2-Amino-4-[(5-methoxypyridin-2-yl)methoxy]phenol (300 mg, 1.16 mmol,prepared using Method 33), 6-fluoropyridine-3-carboxylic acid (180 mg,1.27 mmol) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimidehydrochloride (244 mg, 1.27 mmol) were suspended in pyridine (10 mL).The reaction was stirred at room temperature for 60 hours in a nitrogenatmosphere. The solvents were removed in vacuo and the residuepartitioned between ethyl acetate (100 mL) and water (100 mL), theaqueous was extracted with ethyl acetate (2×50 mL), the combinedorganics were washed with brine (20 mL), dried over anhydrous sodiumsulfate, filtered and concentrated. Purification by FCC (silica, 30-100%ethyl acetate in heptane) gave the title compound, 278 mg (61% yield) asa white powder. Tr(METCR1673)=1.02 min, (ES⁺) (M+H)⁺ 369.

Step 2, Method 61:5-{5-[(5-Methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-1,2-dihydropyridin-2-one

6-Fluoro-N-{2-hydroxy-5-[(5-methoxypyridin-2-yl)methoxy]phenyl}pyridine-3-carboxamide (278 mg, 0.72 mmol) was suspended in acetic acid(5 mL) the reaction was irradiated in the microwave (200 W power, 250psi max) at 180° C. for 30 minutes. The reaction was retreated in themicrowave at 200° C. for 3 hours. The reaction mixture was concentratedin vacuo and the residue partitioned between saturated sodiumbicarbonate solution (50 mL) and ethyl acetate (100 mL), the aqueousextracted with ethyl acetate (2×100 mL), the combined organics washedwith brine (20 mL), dried over anhydrous sodium sulfate, filtered andconcentrated. Purification by FCC (silica, 0-15% methanol indichloromethane) and recrystalisation from DMSO (3 mL) gave the titlecompound, 77.6 mg (30% yield) as a white solid. δ_(H) NMR (500 MHz,DMSO) 12.23 (br. s., 1H), 8.30 (d, J=2.9 Hz, 1H), 8.21 (d, J=2.4 Hz,1H), 8.05 (dd, J=9.6, 2.6 Hz, 1H), 7.60 (d, J=8.9 Hz, 1H), 7.51 (d,J=8.6 Hz, 1H), 7.43 (dd, J=8.6, 3.0 Hz, 1H), 7.35 (d, J=2.5 Hz, 1H),7.02 (dd, J=8.9, 2.5 Hz, 1H), 6.52 (d, J=9.6 Hz, 1H), 5.16 (s, 2H), 3.84(s, 3H). Tr(MET-uHPLC-AB-101)=2.14 min, (ES⁺) (M+H)⁺ 350.

Step 3, Method 61:5-{5-[(5-Methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-1-methyl-1,2-dihydropyridin-2-one

5-{5-[(5-Methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-1,2-dihydropyridin-2-one(42 mg, 0.12 mmol) and methyl 4-nitrobenzenesulfonate (28 mg, 0.13 mmol)were dissolved in anhydrous N,N-dimethylformamide (2 mL) and stirred atroom temperature for 5 minutes. Sodium hydride in mineral oil (60%, 5mg, 0.13 mmol) was added and the reaction stirred at room temperaturefor 2 hours. The reaction was diluted with water (15 mL) and extractedwith ethyl acetate (3×20 mL). The combined organics were washed withbrine (10 mL), dried over anhydrous magnesium sulfate, filtered andconcentrated. The product was purified by FCC (silica, 20-80% premixedtetrahydrofuran:ethyl acetate (2:1) in heptane) and recrystalisationfrom ethanol to give the title compound 8 mg (19% yield) as an off whitepowder.

Example 1, Method 61:5-{5-[(5-Methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-1-methyl-1,2-dihydropyridin-2-one

δ_(H) NMR NMR (500 MHz, DMSO) 8.70 (d, J=2.5 Hz, 1H), 8.30 (d, J=2.9 Hz,1H), 8.04 (dd, J=9.5, 2.6 Hz, 1H), 7.59 (d, J=8.9 Hz, 1H), 7.51 (d,J=8.6 Hz, 1H), 7.42 (dd, J=8.6, 2.9 Hz, 1H), 7.34 (d, J=2.5 Hz, 1H),7.03 (dd, J=8.9, 2.5 Hz, 1H), 6.56 (d, J=9.5 Hz, 1H), 5.16 (s, 2H), 3.83(s, 3H), 3.57 (s, 3H). Tr(MET-uHPLC-AB-101)=2.41 min, (ES⁺) (M+H)⁺ 364.

The following examples were prepared using Method 61 described above:

TABLE 62 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

363.37 5-{5-[(5- methoxypyridin-2- yl)methoxy]-1,3- benzoxazol-2-yl}-1-methyl-1,2- dihydropyridin-2- one Tr(MET-uHPLC- AB-101) = 2.41 min,(ES⁺) (M + H)⁺ 364 2

349.35 5-{5-[(5- methoxypyridin-2- yl)methoxy]-1,3- benzoxazol-2-yl}-1,2-dihydropyridin- 2-one Tr(MET-uHPLC- AB-101) = 2.14 min, (ES⁺) (M +H)⁺ 350Method 62

Step 1, Method 62: 2-(Pyridin-3-yl)-1,3-benzoxazol-5-ol

2-(Pyridin-3-yl)-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3-benzoxazole(0.73 g, 1.58 mmol, prepared using Method 8) was dissolved intetrahydrofuran (10 mL) and water (10 mL), sodium perborate tetrahydrate(0.61 g, 3.95 mmol) was added and the reaction was stirred at roomtemperature in a nitrogen atmosphere for 16 hours. Saturated ammoniumchloride solution (30 mL) was added to the reaction mixture and theproduct was extracted with ethyl acetate (3×100 mL), the combinedorganic extracts were washed with brine (10 mL), dried over anhydrousmagnesium sulfate, filtered and concentrated. Purification by FCC(silica, 20-60% ethyl acetate in heptane, followed by 10% methanol indichloromethane) gave the title compound, 160 mg (48% yield) as a yellowpowder. δ_(H) NMR (500 MHz, DMSO) 9.61 (s, 1H), 9.31 (d, J=2.1 Hz, 1H),8.78 (dd, J=4.8, 1.6 Hz, 1H), 8.49 (dt, J=8.0, 1.9 Hz, 1H), 7.73-7.51(m, 2H), 7.13 (d, J=2.4 Hz, 1H), 6.89 (dd, J=8.8, 2.4 Hz, 1H).Tr(METCR1410)=0.91 min, (ES⁺) (M+H)⁺ 213.

Step 2, Method 62:5-[(5-Bromopyridin-2-yl)methoxy]-2-(pyridin-3-yl)-1,3-benzoxazole

2-(Pyridin-3-yl)-1,3-benzoxazol-5-ol (340 mg, 1.6 mmol) and(5-bromopyridin-2-yl)methanol (349 mg, 1.76 mmol) were suspended inanhydrous toluene (5 mL), cyanomethylenetributylphosphorane (0.63 mL,2.4 mmol) was added and the reaction heated to 100° C. in a sealed tubefor 3 hours. The reaction was cooled to room temperature and thesolvents removed in vacuo. The residue was triturated with diethyl etherand heptane and filtered to give the title compound, 541 mg (87% yield)as a beige solid.

Example 1, Method 62:5-[(5-Bromopyridin-2-yl)methoxy]-2-(pyridin-3-yl)-1,3-benzoxazole

δH NMR (500 MHz, DMSO) 9.47-9.17 (m, 1H), 8.80 (dd, J=4.8, 1.6 Hz, 1H),8.74 (d, J=2.2 Hz, 1H), 8.51 (dt, J=8.0, 1.9 Hz, 1H), 8.11 (dd, J=8.4,2.4 Hz, 1H), 7.75 (d, J=8.9 Hz, 1H), 7.65 (ddd, J=8.0, 4.8, 0.7 Hz, 1H),7.57 (d, J=8.4 Hz, 1H), 7.49 (d, J=2.5 Hz, 1H), 7.16 (dd, J=8.9, 2.6 Hz,1H), 5.26 (s, 2H). Tr(MET-uHPLC-AB-101)=3.44 min, (ES⁺) (M+H)⁺ 382/384.

The following examples were prepared using Method 62 described above:

TABLE 63 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

382.22 5-[(5- Bromopyridin-2- yl)methoxy]-2- (pyridin-3-yl)-1,3-benzoxazole Tr(MET-uHPLC- AB-101) = 3.44 min, (ES⁺) (M + H)⁺ 382/384 2

303.32 5-(Pyridin-2- ylmethoxy)-2- (pyridin-3-yl)-1,3- benzoxazoleTr(MET-uHPLC- AB-101) = 2.3 min, (ES⁺) (M + H)⁺ 304Method 63

Step 1, Method 63:2-Phenyl-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]pyrimidine-5-carboxamide

To a stirred solution of 2-(pyridin-3-yl)-1,3-benzoxazol-5-amine (100mg, 0.47 mmol) in pyridine was added ethylcarbodiimide hydrochloride (91mg, 0.47 mmol) and 2-phenylpyrimidine-5-carboxylic acid (95 mg, 0.47mmol). The reaction mixture was stirred at room temperature for 16hours. Water (10 mL) was added to the reaction mixture and a precipitatewas produced. The precipitate was collected by filtration and dried inan oven for 16 hours to give the title compound 157 mg (84% yield) as atan solid.

Example 1, Method 63:2-Phenyl-N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]pyrimidine-5-carboxamide

δ_(H) NMR (500 MHz, DMSO) 10.82 (s, 1H), 9.40 (s, 2H), 9.37 (s, 1H),8.82 (d, J=4.6 Hz, 1H), 8.55 (d, J=7.8 Hz, 1H), 8.49 (d, J=6.5 Hz, 2H),8.36 (s, 1H), 7.87 (d, J=8.8 Hz, 1H), 7.79 (d, J=8.8 Hz, 1H), 7.67 (dd,J=7.7, 5.0 Hz, 1H), 7.59 (d, J=6.9 Hz, 3H). Tr(MET-uHPLC-AB-101)=3.26min, (ES⁺) (M+H)⁺ 394.

The following examples were prepared using Method 63 described above:

TABLE 64 Mol. Ex. Structure Weight IUPAC Name LCMS data  1

393.41 2-Phenyl-N-[2- (pyridin-3-yl)-1,3- benzoxazol-5- yl]pyrimidine-5-carboxamide Tr(MET-uHPLC- AB-101) = 3.26 min, (ES⁺) (M + H)⁺ 394  2

393.41 N-[2-(Pyridin-3-yl)- 1,3-benzoxazol-5- yl]-4-(pyrimidin-2-yl)benzamide Tr(MET-uHPLC- AB-101) = 2.77 min, (ES⁺) (M + H)⁺ 394  3

355.35 N-[2-(Pyridin-3-yl)- 1,3-benzoxazol-5- yl]-1-benzofuran-5-carboxamide Tr(MET-uHPLC- AB-101) = 2.95 min, (ES⁺) (M + H)⁺ 356  4

319.32 1-Methyl-N-[2- (pyridin-3-yl)-1,3- benzoxazol-5-yl]-1H-pyrazole-4- carboxamide Tr(MET-uHPLC- AB-101) = 1.97 min, (ES⁺) (M +H)⁺ 320  5

423.43 4-[(6- Methylpyrazin-2- yl)oxy]-N-[2- (pyridin-3-yl)-1,3-benzoxazol-5- yl]benzamide Tr(MET-uHPLC- AB-101) = 2.92 min, (ES⁺) (M +H)⁺ 424  6

421.46 4-(Phenoxymethyl)- N-[2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]benzamide Tr(MET-uHPLC- AB-101) = 3.65 min, (ES⁺) (M + H)⁺ 422  7

408.42 2-Phenoxy-N-[2- (pyridin-3-yl)-1,3 benzoxazol-5- yl]pyridine-3-carboxamide Tr(MET-uHPLC- AB-101) = 3.31 min, (ES⁺) (M + H)⁺ 409  8

340.34 4-Cyano-N-[2- (pyridin-3-yl)-1,3- benzoxazol-5- yl]benzamideTr(MET-uHPLC- AB-101) = 2.71 min, (ES⁺) (M + H)⁺ 341  9

346.35 6-Methoxy-N-[2- (pyridin-3-yl)-1,3- benzoxazol-5- yl]pyridine-2-carboxamide Tr(MET-uHPLC- AB-101) = 3.24 min, (ES⁺) (M + H)⁺ 347 10

330.35 2-Methyl-N-[2- (pyridin-3-yl)-1,3- benzoxazol-5- yl]pyridine-4-carboxamide Tr(MET-uHPLC- AB-101) = 1.66 min, (ES⁺) (M + H)⁺ 331 11

346.35 3-Methoxy-N-[2- (pyridin-3-yl)-1,3- benzoxazol-5- yl]pyridine-2-carboxamide Tr(MET-uHPLC- AB-101) = 2.36 min, (ES⁺) (M + H)⁺ 347 12

346.35 4-Methoxy-N-[2- (pyridin-3-yl)-1,3- benzoxazol-5- yl]pyridine-2-carboxamide Tr(MET-uHPLC- AB-101) = 2.85 min, (ES⁺) (M + H)⁺ 347 13

346.35 4-Hydroxy-N-[2- (pyridin-3-yl)-1,3- benzoxazol-5- yl]pyridine-2-carboxamide Tr(MET-uHPLC- AB-101) = 1.91 min, (ES⁺) (M + H)⁺ 333 14

332.32 3-Methoxy-N-[2- (pyridin-3-yl)-1,3- benzoxazol-5-yl]-1,2-oxazole-5- carboxamide Tr(MET-uHPLC- AB-101) = 2.53 min, (ES⁺) (M +H)⁺ 337 15

346.35 5-Methoxy-N-[2- (pyridin-3-yl)-1,3- benzoxazol-5- yl]pyridine-3-carboxamide Tr(MET-uHPLC- AB-101) = 2.17 min, (ES⁺) (M + H)⁺ 347Method 64

Step 1, Method 64:N-(5-Bromo-2-hydroxyphenyl)-1-methyl-1H-pyrazole-4-carboxamide

2-Amino-4-bromophenol (1.4 g, 7.4 mmol),1-methyl-1H-pyrazole-4-carboxylic acid (1.4 g, 11.1 mmol) and1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (3.11 g,16.2 mmol) were suspended in pyridine (30 mL) and the mixture stirred atroom temperature for 64 hours then concentrated to dryness. The residuewas partitioned between ethyl acetate (100 mL) and water (100 mL). Thelayers were separated and the aqueous phase extracted with ethyl acetate(2×50 mL). The combined organic extracts were washed with brine (50 mL),dried over magnesium sulfate, filtered and concentrated. The residue wassuspended in tetrahydrofuran (100 mL) and treated with 2 M sodiumhydroxide (50 mL). After 2 hours the reaction mixture was diluted withethyl acetate (100 mL) and water (30 mL). The layers were separated andthe aqueous phase extracted with ethyl acetate (2×50 mL). Combinedorganic extracts were washed with brine (50 mL), dried over magnesiumsulfate, filtered and evaporated to give the sodium salt of the titlecompound 770 mg (27% yield) as an orange powder. The aqueous wasacidified with 1 M hydrochloric acid (50 mL) and extracted with ethylacetate (2×50 mL). Combined organic extracts were washed with brine (50mL), dried over magnesium sulfate, filtered and evaporated to give thetitle compound 718 mg (19% yield) as an orange powder. δ_(H) NMR (500MHz, DMSO) 10.15 (s, 1H), 9.14 (s, 1H), 8.35 (s, 1H), 7.99 (s, 1H), 7.89(d, J=2.5 Hz, 1H), 7.15 (dd, J=8.6, 2.5 Hz, 1H), 6.86 (d, J=8.6 Hz, 1H),3.89 (s, 3H). Tr(METCR1673)=1.03 min, (ES⁺) (M+H)⁺ 296/298, 58%.

Step 2 Method 64: 5-Bromo-2-(1-methyl-1H-pyrazol-4-yl)-1,3-benzoxazole

N-[5-Bromo-2-(sodiooxy)phenyl]-1-methyl-1H-pyrazole-4-carboxamide (82%,770 mg, 2.13 mmol) was suspended in acetic acid (10 mL) in a pressuretube. N-(5-Bromo-2-hydroxyphenyl)-1-methyl-1H-pyrazole-4-carboxamide(58%, 718 mg, 2.43 mmol) was suspended in acetic acid (10 mL) in apressure tube. Both tubes were sealed and the mixtures heated to 180° C.for 18 hours. Each solution was cooled to room temperature thenconcentrated to dryness. The residues were dissolved in ethyl acetateand combined, then washed with saturated aqueous sodium bicarbonatesolution (20 mL) and brine (20 mL). The organic phase was dried overmagnesium sulfate, filtered and concentrated onto silica. Purificationby FCC (silica, 12-100% ethyl acetate in heptane) gave the titlecompound 572 mg (58% yield) as a light orange powder. δ_(H) NMR (500MHz, DMSO) 8.58 (s, 1H), 8.18-8.07 (m, 1H), 7.92 (d, J=1.9 Hz, 1H), 7.69(d, J=8.6 Hz, 1H), 7.51 (dd, J=8.6, 2.0 Hz, 1H), 3.96 (s, 3H).Tr(MET-uHPLC-AB-101)=2.99 min, (ES⁺) (M+H)⁺ 278/280.

Step 3 Method 64:2-(1-Methyl-1H-pyrazol-4-yl)-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3-benzoxazole

A suspension of 5-bromo-2-(1-methyl-1H-pyrazol-4-yl)-1,3-benzoxazole(560 mg, 2.01 mmol), bis(pinacolato)diboron (562 mg, 2.21 mmol) andpotassium acetate (0.54 g, 5.5 mmol) in anhydrous 1,4-dioxane (25 mL)was degassed with nitrogen for 5 minutes.[1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II) (147 mg,0.20 mmol) was added and the reaction stirred at 100° C. under nitrogenfor 1 hour. The reaction mixture was diluted with methyl tert-butylether (10 mL) and filtered through celite. The filtrate was evaporatedto give a brown residue 1.57 g which was used in the next step withoutpurification. Tr(METCR1673)=1.32 min, (ES⁺) (M+H)⁺ 326, 82%.

Step 4 Method 64: 2-(1-Methyl-1H-pyrazol-4-yl)-1,3-benzoxazol-5-ol

2-(1-Methyl-1H-pyrazol-4-yl)-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3-benzoxazole(1.57 g, assumed 2.01 mmol) was dissolved in 1:1 tetrahydrofuran-water(20 mL). Sodium perborate tetrahydrate (1.54 g, 10.0 mmol) was added andthe mixture stirred at room temperature for 1 hour. Saturated ammoniumchloride solution (20 mL) was added to the reaction mixture and theproduct extracted with ethyl acetate (3×20 mL). The combined organicextracts were washed with brine (15 mL), dried over magnesium sulfate,filtered and evaporated to give a brown solid. Purification by FCC(silica, 25-100% ethyl acetate in heptane) gave the title compound 279mg (32% yield) as an off-white powder. δ_(H) NMR (500 MHz, DMSO) 9.43(s, 1H), 8.50 (s, 1H), 8.06 (s, 1H), 7.47 (d, J=8.7 Hz, 1H), 7.00 (d,J=2.4 Hz, 1H), 6.77 (dd, J=8.7, 2.4 Hz, 1H), 3.95 (s, 3H).Tr(METCR1673)=0.97 min, (ES⁺) (M+H)⁺ 216.

Step 5 Method 64:5-[(5-Bromopyridin-2-yl)methoxy]-2-(1-methyl-1H-pyrazol-4-yl)-1,3-benzoxazole

2-(1-Methyl-1H-pyrazol-4-yl)-1,3-benzoxazol-5-ol (276 mg, 1.28 mmol) and(5-bromopyridin-2-yl)methanol (95%, 279 mg, 1.41 mmol) were suspended inanhydrous toluene (10 mL). Cyanomethylenetributylphosphorane (505 μl,1.92 mmol) was added and the mixture heated to 100° C. under nitrogenfor 2 hours. The reaction mixture was cooled to room temperature andconcentrated. The residue was triturated with heptane-diethyl ether(1:1, 20 mL) and the solid collected by filtration and dried undersuction to give the title compound 410 mg (79% yield) as a light brownpowder. δ_(H) NMR (500 MHz, DMSO) 8.73 (d, J=2.2 Hz, 1H), 8.52 (s, 1H),8.10 (dd, J=8.4, 2.4 Hz, 1H), 8.08 (s, 1H), 7.61 (d, J=8.8 Hz, 1H), 7.55(d, J=8.4 Hz, 1H), 7.33 (d, J=2.5 Hz, 1H), 7.03 (dd, J=8.8, 2.5 Hz, 1H),5.22 (s, 2H), 3.95 (s, 3H). Tr(METCR1673)=1.25 min, (ES⁺) (M+H)⁺385/387.

Step 6 Method 64:2-(1-Methyl-1H-pyrazol-4-yl)-5-{[5-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]methoxy}-1,3-benzoxazole

A suspension of5-[(5-bromopyridin-2-yl)methoxy]-2-(1-methyl-1H-pyrazol-4-yl)-1,3-benzoxazole(410 mg, 1.06 mmol), bis(pinacolato)diboron (297 mg, 1.17 mmol) andpotassium acetate (261 mg, 2.66 mmol) in anhydrous 1,4-dioxane (15 mL)was degassed with nitrogen for 5 minutes.Bis(diphenylphosphino)ferrocene]dichloropalladium(II) (78 mg, 0.11 mmol)was added and the reaction stirred at 100° C. under nitrogen for 17hours. The reaction mixture was diluted with tert-butyl methyl ether (20mL), filtered and concentrated. The residue was triturated in 1:1heptane: tert-butyl methyl ether and filtered to give the title compound479 mg (100% yield) as a grey powder. δ_(H) NMR (500 MHz, DMSO) 8.77 (s,1H), 8.52 (s, 1H), 8.08 (s, 111), 8.05 (dd, J=7.8, 1.7 Hz, 1H), 7.60 (d,J=8.8 Hz, 1H), 7.57 (d, J=7.7 Hz, 1H), 7.31 (d, J=2.5 Hz, 1H), 7.03 (dd,J=8.9, 2.6 Hz, 1H), 5.27 (s, 2H), 3.95 (s, 3H), 1.31 (s, 12H).Tr(METCR1673)=0.91 min, (ES⁺) (M+H)⁺ 351 [corresponding boronic acid].

Step 7 Method 64:6-({[2-(1-Methyl-1H-pyrazol-4-yl)-1,3-benzoxazol-5-yl]oxy}methyl)pyridin-3-ol

2-(1-Methyl-1H-pyrazol-4-yl)-5-{[5-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]methoxy}-1,3-benzoxazole(479 mg, 1.11 mmol) was dissolved in 1:1 tetrahydrofuran-water (10 mL).Sodium perborate tetrahydrate (426 mg, 2.8 mmol) was added and themixture stirred at room temperature for 1 hour. Saturated ammoniumchloride solution (20 mL) was added to the reaction mixture and themixture extracted with ethyl acetate (3×20 mL). The combined organicextracts were washed with brine (15 mL), dried over magnesium sulfate,filtered and concentrated. The residue was triturated inheptane-tert-butyl methyl ether/ethyl acetate and filtered. The filtratestood at room temperature overnight, forming crystals. The mother liquorwas decanted off and the crystals were suspended in heptane andcollected by filtration. Drying under suction gave the title compound114 mg (32% yield) as brown crystals.

Example 1, Method 64:6-({[2-(1-Methyl-1H-pyrazol-4-yl)-1,3-benzoxazol-5-yl]oxy}methyl)pyridin-3-ol

δH NMR (500 MHz, DMSO) 9.97 (s, 1H), 8.51 (s, 1H), 8.13 (d, J=2.7 Hz,1H), 8.08 (s, 1H), 7.58 (d, J=8.8 Hz, 1H), 7.39 (d, J=8.4 Hz, 1H), 7.31(d, J=2.5 Hz, 1H), 7.19 (dd, J=8.4, 2.8 Hz, 1H), 6.99 (dd, J=8.8, 2.5Hz, 1H), 5.09 (s, 2H), 3.95 (s, 3H). Tr(MET-uHPLC-AB-101)=1.87 min,(ES⁺) (M+H)⁺ 323.

The following examples were prepared using Method 64 described above:

TABLE 65 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

322.32 6-({[2-(1-Methyl- 1H-pyrazol-4-yl)- 1,3-benzoxazol-5-yl]oxy}methyl) pyridin-3-ol Tr(MET-uHPLC- AB-101) = 1.87 min, (ES⁺) (M +H)⁺ 323 2

337.34 5-[(5- Methoxypyrazin-2- yl)methoxy]-2-(1- methyl-1H- pyrazol-4-yl)-1,3- benzoxazole Tr(MET-uHPLC- AB-101) = 2.83 min, (ES⁺) (M + H)⁺338Method 65

Step 1, Method 65:3-{16-[(5-Bromopyridin-2-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine

To a suspension of 2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-ol (120mg, 0.56 mmol, prepared using Method 30) and(5-bromopyridin-2-yl)methanol (95%, 123 mg, 0.62 mmol) in toluene (3 mL)was added cyanomethylenetributylphosphorane (0.25 mL, 0.95 mmol) andmixture heated at 100° C. for 3 hours in a sealed tube. After coolingthe mixture was distributed between ethyl acetate (300 mL) and saturatedsodium hydrogen carbonate solution (100 mL). The organic layer waswashed with brine (50 mL), dried over magnesium sulfate, filtered andevaporated. The solid residue was triturated with ethyl acetate (˜5 mL)and then re-crystallised from a hot mixture of tetrahydrofuran andacetonitrile (˜5 mL, 1:1) to provide the title compound 74 mg (34%yield) as an off-white solid. δ_(H) NMR (500 MHz, DMSO) 9.40-9.26 (m,1H), 8.83 (dd, J=4.8, 1.6 Hz, 1H), 8.74 (d, J=2.3 Hz, 1H), 8.54 (dt,J=8.0, 1.9 Hz, 1H), 8.25 (d, J=2.7 Hz, 1H), 8.13 (dd, J=8.4, 2.4 Hz,1H), 8.08 (d, J=2.7 Hz, 1H), 7.73-7.64 (m, 1H), 7.60 (d, J=8.4 Hz, 1H),5.33 (s, 2H). Tr(MET-uHPLC-AB-101)=3.08 min, (ES⁺) (M+H)⁺ 383, 385

Step 2, Method 65:5-(1-Methyl-1H-pyrazol-4-yl)-2-({[2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)pyridine

3-{6-[(5-Bromopyridin-2-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine(69 mg, 0.16 mmol), (1-methyl-1H-pyrazol-4-yl)boronic acid (22 mg, 0.18mmol) and 2 M sodium carbonate (0.16 mL) were suspended in anhydrous1,2-dimethoxyethane (1 mL) and anhydrous ethanol (1 mL) and degassedunder a flow of nitrogen for 5 minutes. Palladium tetrakistriphenylphosphine(0) (9 mg, 0.01 mmol) was added and the reaction washeated to 90° C. in a sealed tube for 2 hours.(1-Methyl-1H-pyrazol-4-yl)boronic acid (22 mg, 0.18 mmol) and palladiumtetrakis triphenylphosphine(0) (9 mg, 0.01 mmol) were added and thereaction was heated to 90° C. for 2 hours. The reaction mixture wascooled to room temperature and partitioned between ethyl acetate (100mL) and water (50 mL), a precipitate was filtered from the mixture andtriturated with hot ethanol, filtered and washed with diethyl ether togive the title compound 39 mg (56% yield) as a grey solid.

Example 1, Method 65:5-(1-Methyl-1H-pyrazol-4-yl)-2-({[2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)pyridine

δ_(H) NMR (500 MHz, DMSO) 9.35 (d, J=1.7 Hz, 1H), 8.85 (d, J=2.0 Hz,1H), 8.83 (dd, J=4.8, 1.6 Hz, 1H), 8.55 (dt, J=8.0, 1.9 Hz, 1H), 8.27(s, 1H), 8.25 (d, J=2.7 Hz, 1H), 8.10 (d, J=2.7 Hz, 1H), 8.02 (dd,J=8.1, 2.3 Hz, 1H), 7.98 (s, 1H), 7.67 (dd, J=8.0, 4.8 Hz, 1H), 7.59 (d,J=8.1 Hz, 1H), 5.33 (s, 2H), 3.88 (s, 3H). Tr(MET-uHPLC-AB-101)=2.25min, (ES⁺) (M+H)⁺ 385.

The following examples were prepared using Method 65 described above:

TABLE 66 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

384.40 5-(1-Methyl-1H- pyrazol-4-yl)-2- ({[2-(pyridin-3-yl)-[1,3]oxazolo[5,4- b]pyridin-6- yl]oxy}methyl) pyridine Tr(MET-uHPLC-AB-101) = 2.25 min, (ES⁺) (M + H)⁺ 385 2

383.21 3-{6-[(5- Bromopyridin-2- yl)methoxy]- [1,3]oxazolo[5,4-b]pyridin-2- yl}pyridine Tr(MET-uHPLC- AB-101) = 3.08 min, (ES⁺) (M +H)⁺ 383/385 3

335.32 3-Methoxy-6-({[2- (pyridin-3-yl)- [1,3]oxazolo[5,4- b]pyridin-6-yl]oxy}methyl) pyridazine Tr(MET-uHPLC- AB-101) = 2.31 min, (ES+) (M +H)+ 336Method 66

Step 1, Method 66:3-{5-[(5-Methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}benzonitrile

2-Amino-4-[(5-methoxypyridin-2-yl)methoxy]phenol (190 mg, 0.77 mmol,prepared using Method 33) was dissolved in methanol (10 mL),3-formylbenzonitrile (70 mg, 0.53 mmol) added and the reaction mixturestirred at room temperature for 90 minutes. The methanol was thenremoved in vacuo and the residue dissolved in dichloromethane (25 mL),cooled to 0° C. and 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (205 mg,0.9 mmol) added. The ice bath was removed and the mixture was stirred atroom temperature for 2 hours, then diluted with dichloromethane (100 mL)and filtered. The solid was washed with dichloromethane (2×50 mL) andthe washings and the filtrate combined, dried over magnesium sulfate,filtered and concentrated. Purification by FCC (silica, 0-80% ethylacetate in heptane) and trituration with ethanol gave the title compound(65.2 mg, 34% yield) as an off-white solid.

Example 1, Method 66:3-{5-[(5-Methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}benzonitrile

δ_(H) NMR (500 MHz, DMSO) 8.53 (s, 1H), 8.47 (d, J=8.0 Hz, 1H), 8.31 (d,J=2.9 Hz, 1H), 8.09 (d, J=7.8 Hz, 1H), 7.83 (t, J=7.9 Hz, 1H), 7.73 (d,J=8.9 Hz, 1H), 7.53 (d, J=8.6 Hz, 1H), 7.48 (d, J=2.5 Hz, 1H), 7.43 (dd,J=8.6, 3.0 Hz, 1H), 7.15 (dd, J=8.9, 2.5 Hz, 1H), 5.19 (s, 2H), 3.84 (s,3H). Tr(MET-uHPLC-AB-101)=3.49 min, (ES⁺) (M+H)⁺ 358.

The following examples were prepared using Method 66 described above:

TABLE 67 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

357.37 3-{5-[(5- Methoxypyridin-2- yl)methoxy]-1,3- benzoxazol-2-yl}benzonitrile Tr(MET-uHPLC- AB-101) = 3.49 min, (ES⁺) (M + H)⁺ 358 2

357.37 4-{5-[(5- Methoxypyridin-2- yl)methoxy]-1,3- benzoxazol-2-yl}benzonitrile Tr(MET-uHPLC- AB-101) = 3.45 min, (ES⁺) (M + H)⁺ 358Method 67

Step 1, Method 67:3-Methoxy-5-({[2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)pyridine

2-(Pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-ol (86%, 100 mg, 0.4 mmol,prepared using Method 30) and (5-methoxypyridin-3-yl)methanol (65 mg,0.44 mmol) were suspended in anhydrous toluene (3 mL).Cyanomethylenetributylphosphorane (0.16 mL, 0.61 mmol) was added and thereaction heated to 100° C. in a sealed tube for 18 hours. The reactionwas cooled to room temperature and the solvents removed in vacuo. Theresidue was triturated with diethyl ether and heptane. Purification byFCC (silica, 0-10% methanol in dichloromethane) gave the title compound45 mg (33% yield) as an off white solid.

Example 1, Method 67:3-Methoxy-5-({[2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)pyridine

δ_(H) NMR (500 MHz, DMSO) 9.35 (d, J=2.0 Hz, 1H), 8.83 (dd, J=4.8, 1.5Hz, 1H), 8.55 (dt, J=8.0, 1.9 Hz, 1H), 8.32 (d, J=1.2 Hz, 1H), 8.29 (d,J=2.8 Hz, 1H), 8.24 (d, J=2.7 Hz, 1H), 8.11 (d, J=2.7 Hz, 1H), 7.67(ddd, J=8.0, 4.8 Hz, 1H), 7.54 (s, 1H), 5.31 (s, 2H), 3.86 (s, 3H).Tr(MET-uHPLC-AB-101)=1.94 min, (ES⁺) (M+H)⁺ 335.

The following examples were prepared using Method 67 described above:

TABLE 68 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

334.34 3-Methoxy-5-({[2- (pyridin-3-yl)- [1,3]oxazolo[5,4- b]pyridin-6-yl]oxy}methyl) pyridine Tr(MET-uHPLC- AB-101) = 1.94 min, (ES⁺) (M + H)⁺335 2

334.34 4-Methoxy-2-({[2- (pyridin-3-yl)- [1,3]oxazolo[5,4- b]pyridin-6-yl]oxy}methyl) pyridine Tr(MET-uHPLC- AB-101) = 1.47 min, (ES⁺) (M + H)⁺335 3

308.30 2-({[2-(1-Methyl- 1H-pyrazol-4-yl)- [1,3]oxazolo[5,4-b]pyridin-6- yl]oxy}methyl) pyrazine Tr(MET-uHPLC- AB-101) = 1.99 min,(ES⁺) (M + H)⁺ 309Method 68

Step 1, Method 68:3-Formyl-N-{2-hydroxy-5-[(5-methoxypyridin-2-yl)methoxy]phenyl}benzamide

To a solution of 3-formylbenzoic acid (61 mg, 0.41 mmol),2-amino-4-[(5-methoxypyridin-2-yl)methoxy] phenol (112 mg, 0.45 mmol) inpyridine (5 mL) was added ethylcarbodiimide hydrochloride (104 mg, 0.55mmol) and the resulting mixture stirred overnight at room temperature.The solvent was evaporated and the residue portioned betweendichloromethane and water, the dichloromethane layer separated, driedover sodium sulfate, filtered and concentrated to give the crudeproduct, which was used in the next step without further purification.

Step 2, Method 68:3-{5-[(5-Methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}benzaldehyde

A solution of3-formyl-N-{2-hydroxy-5-[(5-methoxypyridin-2-yl)methoxy]phenyl}benzamide(178 mg, 0.38 mmol, circa 80% purity) in acetic acid (4 mL) was heatedto 180° C. in a microwave for 50 mins. The mixture was diluted withwater and aqueous sodium hydrogen carbonate solution added to give pH 8,the aqueous layer extracted with dichloromethane (100 mL) and thecombined organic layers dried over sodium sulfate, filtered andconcentrated. Purification by preparative HPLC (acetonitrile/water+0.1%formic acid) gave the title compound 34 mg (25% yield over two steps) asan off-white solid. δ_(H) NMR (500 MHz, chloroform) 10.15 (s, 1H), 8.73(s, 1H), 8.50 (d, J=7.8 Hz, 1H), 8.34 (d, J=2.8 Hz, 1H), 8.06 (d, J=7.7Hz, 1H), 7.72 (t, J=7.7 Hz, 1H), 7.52 (d, J=8.9 Hz, 1H), 7.49 (d, J=8.6Hz, 1H), 7.37 (d, J=2.5 Hz, 1H), 7.26 (dd, J=8.6, 2.9 Hz, 1H), 7.11 (dd,J=8.9, 2.5 Hz, 1H), 5.24 (s, 2H), 3.90 (s, 3H). Tr(METCR1678)=1.29 min(ES⁺) (M+H)⁺ 361.

Step 3, Method 68:[(3-{5-[(5-Methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2yl}phenyl)methyl](methyl)amine

To a solution of3-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}benzaldehyde(34 mg, 0.09 mmol) in toluene (5 mL) was added methylamine solution inethanol (33 wt %, 0.5 mL) and the volatiles evaporated. The residue wasdissolved in toluene and a further charge of methylamine solution inethanol (33 wt %, 0.5 mL) added, along with magnesium sulfate. Themixture was stirred for 15 mins, filtered and concentrated to give thecrude imine, which was redissolved in 1,2-dichloroethane (5 mL). Sodiumtriacetoxyborohydride (30 mg, 0.14 mmol) and one drop of acetic acidwere added and the reaction mixture stirred overnight. The mixture wasdiluted with water, aqueous sodium hydrogen carbonate solution added andthe organic layer separated, dried over sodium sulfate, filtered andconcentrated. Purification by FCC (silica, dichloromethane:methanol:7 Mmethanolic ammonia (98:1.5:0.5)) gave the title compound 19 mg (54%yield) as an off-white solid.

Example 1, Method 68:[(3-{5-[(5-Methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2yl}phenyl)methyl](methyl)amine

δ_(H) NMR (500 MHz, DMSO) 8.30 (d, J=2.7 Hz, 1H), 8.16 (s, 1H), 8.04 (d,J=6.6 Hz, 1H), 7.69 (d, J=8.9 Hz, 1H), 7.60-7.48 (m, 3H), 7.43 (m, 2H),7.10 (dd, J=8.9, 2.4 Hz, 1H), 5.18 (s, 2H), 3.84 (s, 3H), 3.78 (s, 2H),2.31 (s, 3H). Tr(METCR1600)=4.47 min (ES⁺) (M+H)⁺ 376.

The following example was prepared using Method 68 described above:

TABLE 69 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

375.43 [(3-{5-[(5- Methoxypyridin-2- yl)methoxy]-1,3- benzoxazol-2-yl}phenyl)methyl] (methyl)amine Tr(METCR1600) = 4.47 min, (ES⁺) (M + H)⁺376Method 69

Step 1, Method 69: (5-Methoxypyridin-2-yl)methylN-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]carbamate

(5-Methoxypyridin-2-yl)methanol (66 mg, 0.47 mmol) andcarbonyldiimidazole (92 mg, 0.57 mmol) were dissolved in dichloromethane(2 mL) and stirred at room temperature for 4 hours.2-(Pyridin-3-yl)-1,3-benzoxazol-5-amine (100 mg, 0.47 mmol) was addedand the reaction mixture stirred at room temperature for 24 hours. Thereaction mixture was diluted with ethyl acetate (25 mL), washed withwater (3×20 mL), dried over anhydrous magnesium sulfate, filtered andconcentrated. Purification by preparative HPLC (acetonitrile/water+0.1%formic acid) gave the title compound 12.3 mg (7% yield) as a pale pinksolid

Example 1, Method 69: (5-Methoxypyridin-2-yl)methylN-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]carbamate

δ_(H) NMR (500 MHz, DMSO) 10.02 (s, 1H), 9.33 (d, J=1.6 Hz, 1H), 8.80(dd, J=4.8, 1.6 Hz, 1H), 8.52 (dt, J=8.0, 1.9 Hz, 1H), 8.29 (dd, J=2.7,0.8 Hz, 1H), 8.00 (s, 1H), 7.75 (d, J=8.8 Hz, 1H), 7.65 (ddd, J=8.0,4.9, 0.8 Hz, 1H), 7.52-7.38 (m, 3H), 5.18 (s, 2H), 3.84 (s, 3H).Tr(MET-uHPLC-AB-101)=2.38 min, (ES⁺) (M+H)⁺ 377.

The following example was prepared using Method 69 described above:

TABLE 70 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

376.37 (5-Methoxypyridin- 2-yl)methyl N-[2- (pyridin-3-yl)-1,3-benzoxazol-5- yl]carbamate Tr(MET-uHPLC- AB-101) = 2.38 min, (ES⁺) (M +H)⁺ 377Method 70

Step 1, Method 70:N-{2-Hydroxy-5-[(5-methoxypyridin-2-yl)methoxy]phenyl}-5-methoxypyridine-2-carboxamide

To a solution of 2-Amino-4-[(5-methoxypyridin-2-yl)methoxy]phenol (80%,100 mg, 0.32 mmol, prepared using Method 33) in pyridine was added5-methoxypyridine-2-acid chloride (55 mg, 0.32 mmol). The reactionmixture was stirred at room temperature for two days. Pyridine wasremoved in vacuo and the residue taken up in dichloromethane (30 mL).This was washed with water (2×25 mL), brine (15 mL), dried overmagnesium sulfate, filtered and concentrated to give the title compound130 mg (67% yield) as a red solid. The crude material was taken directlyinto the next step.

Step 2, Method 70:2-(5-Methoxypyridin-2-yl)-5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazole

N-{2-Hydroxy-5-[(5-methoxypyridin-2-yl)methoxy]phenyl}-5-methoxypyridine-2-carboxamide(130 mg, 0.27 mmol) was taken up in acetic acid (3 mL) and heated in amicrowave at 200° C. for 1 hour. The acetic acid was removed in vacuoand the residue dissolved in dichloromethane (30 mL). The organic layerwas washed with saturated sodium hydrogen carbonate solution (2×30 mL),brine (15 mL) and dried over magnesium sulfate. The magnesium sulfatewas filtered off and dichloromethane removed in vacuo. Purification byFCC (silica, 0-10% methanol in dichloromethane) followed byrecrystalisation from ethanol gave the title compound 6.6 mg, (7% yield)as an off white solid.

Example 1, Method 70:2-(5-Methoxypyridin-2-yl)-5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazole

δ_(H) NMR (500 MHz, DMSO) 8.48 (d, J=2.8 Hz, 1H), 8.31 (d, J=2.8 Hz,1H), 8.27 (d, J=8.8 Hz, 1H), 7.71 (d, J=8.9 Hz, 1H), 7.62 (dd, J=8.8,2.9 Hz, 1H), 7.53 (d, J=8.6 Hz, 1H), 7.49-7.41 (m, 2H), 7.11 (dd, J=8.9,2.5 Hz, 1H), 5.19 (s, 2H), 3.95 (s, 3H), 3.84 (s, 3H).Tr(MET-uHPLC-AB-101)=2.82 min, (ES⁺) (M+H)⁺ 364.

The following example was prepared using Method 70 described above:

TABLE 71 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

363.37 2-(5-Methoxypyridin- 2-yl)-5-[(5- methoxypyridin-2-yl)methoxy]-1,3- benzoxazole Tr(MET-uHPLC- AB-101) = 2.82 min, (ES⁺)(M + H)⁺ 364 2

372.38 2-(1-Benzofuran-2-yl)- 5-[(5-methoxypyridin- 2-yl)methoxy]-1,3-benzoxazole Tr(MET-uHPLC- AB-101) = 4.04 min, (ES⁺) (M + H)⁺ 373 3

401.35 5-[(5-Methoxypyridin- 2-yl)methoxy]-2-[6- (trifluoromethyl)pyridin-3-yl]-1,3- benzoxazole Tr(METCR1416 Hi res 7 min) = 4.36 min,(ES⁺) (M + H)⁺ 402 4

372.38 2-(1-Benzofuran-5-yl)- 5-[(5-methoxypyridin- 2-yl)methoxy]-1,3-benzoxazole Tr(MET-uHPLC- AB-101) = 3.76 min, (ES⁺) (M + H)⁺ 373 5

383.41 2-{5-[(5- Methoxypyridin-2- yl)methoxy]-1,3- benzoxazol-2-yl}quinoline Tr(MET-uHPLC- AB-101) = 3.46 min, (ES⁺) (M + H)⁺ 384 6

438.48 2-[3- (Benzyloxy)phenyl]-5- [(5-methoxypyridin-2-yl)methoxy]-1,3- benzoxazole Tr(MET-uHPLC- AB-101) = 4.44 min, (ES⁺)(M + H)⁺ 439 7

410.43 5-[(5-Methoxypyridin- 2-yl)methoxy]-2-[4- (pyrimidin-2-yl)phenyl]-1,3- benzoxazole Tr(MET-uHPLC- AB-101) = 3.63 min, (ES⁺) (M +H)⁺ 411 8

388.42 2-[(E)-2-(4- Methoxyphenyl) ethenyl]-5-[(5- methoxypyridin-2-yl)methoxy]-1,3- benzoxazole Tr(MET-uHPLC- AB-101) = 3.81 min, (ES⁺)(M + H)⁺ 389Method 71

Step 1, Method 71: Methyl 5-methoxypyrimidine-2-carboxylate

To a round bottom flask were added sequentially methyl5-bromopyrimidine-2-carboxylate (0.83 g, 3.82 mmol),di-tert-butyl({3,6-dimethoxy-2-[2,4,6-tris(propan-2-yl)phenyl]phenyl})phosphane(0.02 g, 0.04 mmol) and caesium carbonate (1.74 g, 5.35 mmol). Thesesolids were mixed, then evacuated under vacuum and purged with nitrogenthree times. Methanol (0.61 g, 19.12 mmol) was then added to this flaskvia a syringe. In a separate flask was weighedmethanesulfonato(2-(di-tert-butylphosphino)-3,6-dimethoxy-2′,4′,6′-tri-i-propyl-1,1′-biphenyl)(2′-amino-1,1′-biphenyl-2-yl)palladium(II)(0.03 g, 0.04 mmol), which was evacuated and purged with nitrogen twice.Dioxane (3.8 mL) was added to this flask and the flask agitated until agreenish solution resulted; this solution was then transferred viasyringe to the first flask. The resulting reaction mixture was heated to50° C. for 4 hours. The reaction mixture was cooled, diluted with ethylacetate and filtered. The volatiles were evaporated and the residuepurified by FCC (silica, 50-100% ethyl acetate in heptane) to give thetitle compound 0.25 g (32% yield) as an off-white solid. δ_(H) NMR (500MHz, Chloroform) 8.54 (s, 2H), 4.05 (s, 3H), 4.01 (s, 3H).Tr(METCR1673)=0.48 min, (ES⁺) (M+H)⁺ 169.

Step 2, Method 71: (5-Methoxypyrimidin-2-yl)methanol

To a solution of methyl 5-methoxypyrimidine-2-carboxylate (180 mg, 1.07mmol) in ethanol (4 mL) was added sodium borohydride (81 mg, 2.14 mmol)and the resulting mixture stirred for 90 mins. The volatiles wereevaporated, the residue diluted with ethyl acetate and filtered througha pad of silica. Evaporation gave the title compound 35 mg (23% yield)as a pale yellow solid. δ_(H) NMR (500 MHz, Chloroform) 8.40 (s, 2H),4.79 (s, 2H), 3.93 (s, 3H).

Step 3, Method 71:5-Methoxy-2-({[2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)pyrimidine

A mixture of (5-methoxypyrimidin-2-yl)methanol (26 mg, 0.19 mmol),2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-ol (90%, 44 mg, 0.19 mmol,prepared using Method 30) and cyanomethylenetributylphosphorane (0.07mL, 0.28 mmol) in toluene (1 mL) was heated to reflux for 6 hours. Thereaction mixture was evaporated and purified by FCC (silica, 2-35%tetrahydrofuran in dichloromethane), triturated with ether (5 mL) andair-dried to give the title compound 13.1 mg (21% yield) as a lightbrown solid.

Example 1, Method 71:5-Methoxy-2-({[2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)pyrimidine

δ_(H) NMR (500 MHz, DMSO) 9.35 (dd, J=2.2, 0.7 Hz, 1H), 8.83 (dd, J=4.8,1.6 Hz, 1H), 8.60 (s, 2H), 8.57-8.51 (m, 1H), 8.20 (d, J=2.7 Hz, 1H),8.03 (d, J=2.7 Hz, 1H), 7.67 (ddd, J=8.0, 4.8, 0.8 Hz, 1H), 5.39 (s,2H), 3.92 (s, 3H). Tr(MET-uHPLC-AB-101)=2.18 min, (ES⁺) (M+H)⁺ 336.

The following example was prepared using Method 71 described above:

TABLE 72 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

335.32 5-Methoxy-2-({[2- (pyridin-3-yl)- [1,3]oxazolo[5,4- b]pyridin-6-yl]oxy}methyl) pyrimidine Tr(MET-uHPLC- AB-101) = 2.18 min, (ES⁺) (M +H)⁺ 336Method 72

Step 1, Method 72:2-[6-(Hydroxymethyl)pyridin-3-yl]-2,3-dihydro-1H-isoindole-1,3-dione

5-Aminopyridin-2-yl)methanol dihydrochloride (500 mg, 2.54 mmol) and2-benzofuran-1,3-dione (376 mg, 2.54 mmol) were refluxed with stirringin pyridine (10 mL) for 4 hours under nitrogen. The mixture wasevaporated and recrystallised from methanol (20 mL) to give the titlecompound 314 mg (48.7% yield) as an off white powder. δ_(H) NMR (500MHz, DMSO) 8.57 (d, J=2.3 Hz, 1H), 8.03-7.96 (m, 2H), 7.96-7.92 (m, 2H),7.90 (dd, J=8.3, 2.4 Hz, 1H), 7.64 (d, J=8.3 Hz, 1H), 5.53 (t, J=5.9 Hz,1H), 4.63 (d, J=5.7 Hz, 2H). Tr(METCR1673 2 min method)=0.94 min, (ES⁺)(M+H)⁺ 255.

Step 2, Method 72:2-[6-({[2-(1-Methyl-1H-pyrazol-4-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)pyridin-3-yl]-2,3-dihydro-1H-isoindole-1,3-dione

2-(1-Methyl-1H-pyrazol-4-yl)-[1,3]oxazolo[5,4-b]pyridin-6-ol (61 mg,0.28 mmol, prepared using Method 30),2-[6-(hydroxymethyl)pyridin-3-yl]-2,3-dihydro-1H-isoindole-1,3-dione (79mg, 0.31 mmol) and cyanomethylenetributylphosphorane (111 μl, 0.42 mmol)in toluene (5 mL) were heated to 100° C. under nitrogen overnight.Cyanomethylenetributylphosphorane (111 μl, 0.42 mmol) in toluene (5 mL)was added and the mixture heated to 120° C. under nitrogen overnight.The reaction mixture was cooled to room temperature and concentrated.Trituration with diethyl ether (10 mL) gave a tan solid 62 mg 36% purityby LC-MS but ˜90% by proton NMR and the crude material was taken on tothe next step.

Step 3, Method 72:6-({[2-(1-Methyl-1H-pyrazol-4-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)pyridin-3-amine

2-[6-({[2-(1-Methyl-1H-pyrazol-4-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)pyridin-3-yl]-2,3-dihydro-1H-isoindole-1,3-dione(90%, 62 mg, 0.12 mmol) was suspended in ethanol (2 mL) and hydrazinehydrate (1:1) (120.24 μl, 2.47 mmol) added and the mixture stirred atroom temperature overnight. The mixture was filtered, and the solidwashed with methanol (5 mL) and ethyl acetate (5 mL). The filtrate wasconcentrated and purified by preparative HPLC (acetonitrile/water+0.2%ammonium hydroxide) followed by recrystalisation from methanol (1 mL)gave the title compound 10 mg (24% yield) as an off white powder.

Example 1, Method 72:6-({[2-(1-Methyl-1H-pyrazol-4-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)pyridin-3-amine

δ_(H) NMR (500 MHz, DMSO) 8.59 (s, 1H), 8.13 (s, 1H), 8.02 (d, J=2.7 Hz,1H), 7.93 (d, J=2.6 Hz, 1H), 7.85 (d, J=2.7 Hz, 1H), 7.22 (d, J=8.3 Hz,1H), 6.94 (dd, J=8.3, 2.7 Hz, 1H), 5.40 (s, 2H), 5.07 (s, 2H), 3.96 (s,3H). Tr(MET-uHPLC-AB-101)=1.31 min, (ES⁺) (M+H)⁺ 323.

The following example was prepared using Method 72 described above:

TABLE 73 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

322.33 6-({[2-(1-Methyl- 1H-pyrazol-4-yl)- [1,3]oxazolo[5,4-b]pyridin-6-yl]oxy} methyl)pyridin-3- amine Tr(MET-uHPLC- AB-101) = 1.31min, (ES⁺) (M + H)⁺ 323Method 73

Step 1, Method 73:2-Methyl-5-{[5-(prop-2-en-1-yloxy)pyridin-2-yl]methoxy}-1,3-benzoxazole

2-Methyl-1,3-benzoxazol-5-ol (1.4 g, 9.39 mmol) and[5-(prop-2-en-1-yloxy)pyridin-2-yl]methanol (1.8 g, 10.33 mmol,described in U.S. Pat. No. 4,198,416 (1978) reference example 3) weresuspended in anhydrous toluene (20 mL),cyanomethylenetributylphosphorane (3.69 mL, 14.08 mmol) added and thereaction heated to 100° C. for 4 hours under nitrogen. The reaction wascooled to room temperature and the solvent removed in vacuo. Triturationwith diethyl ether and heptane (1:1, 10 mL) gave the title compound1.449 g (52% yield) as a purple solid. δ_(H) NMR (250 MHz, DMSO) 8.31(d, J=2.3 Hz, 1H), 7.55 (d, J=8.9 Hz, 1H), 7.49 (d, J=8.4 Hz, 1H), 7.43(dd, J=8.6, 2.8 Hz, 1H), 7.29 (d, J=2.5 Hz, 1H), 7.00 (dd, J=8.9, 2.6Hz, 1H), 6.05 (ddt, J=17.2, 10.5, 5.2 Hz, 1H), 5.42 (dq, J=17.3, 1.7 Hz,1H), 5.29 (dq, J=10.5, 1.4 Hz, 1H), 5.14 (s, 2H), 4.67 (dt, J=5.2, 1.4Hz, 2H), 2.58 (s, 3H) Tr(METCR1673)=1.26 min, (ES⁺) (M+H)⁺ 297.

Step 2, Method 73:2-Amino-4-{[5-(prop-2-en-1-yloxy)pyridin-2-yl]methoxy}phenol

2-Methyl-5-{[5-(prop-2-en-1-yloxy)pyridin-2-yl]methoxy}-1,3-benzoxazole(98%, 1.7 g, 5.61 mmol) was dissolved in ethanol (30 mL) and 2 Mhydrochloric acid (15 mL) added and the reaction heated to 105° C. for40 hours. The reaction mixture was cooled to room temperature and thesolvent removed in vacuo. The residue was sonicated with saturatedsodium bicarbonate solution, adjusting the pH to 8 and then partitionedwith dichloromethane (100 mL) and the layers separated. The aqueouslayer was extracted with dichloromethane (2×75 mL). The combinedorganics were washed with brine (20 mL), dried over anhydrous sodiumsulfate, and concentrated in vacuo to give the title compound 1.17 g(76% yield) as a bronze solid. δ_(H) NMR (500 MHz, DMSO) 8.48 (s, 1H),8.26 (d, J=2.2 Hz, 1H), 7.46-7.34 (m, 2H), 6.50 (d, J=8.5 Hz, 1H), 6.27(d, J=2.9 Hz, 1H), 6.12-5.96 (m, 2H), 5.41 (dd, J=17.3, 1.7 Hz, 1H),5.28 (dd, J=10.5, 1.5 Hz, 1H), 4.90 (s, 2H), 4.65 (dt, J=5.2, 1.4 Hz,2H), 4.53 (s, 2H). Tr(METCR1673)=0.87 min, (ES⁺) (M+H)⁺ 273, 93%.

Step 3, Method 73:N-(2-Hydroxy-5-{[5-(prop-2-en-1-yloxy)pyridin-2-yl]methoxy}phenyl)-1-methyl-6-oxo-1,6-dihydropyridazine-3-carboxamide

To a solution of2-amino-4-{[5-(prop-2-en-1-yloxy)pyridin-2-yl]methoxy}phenol (835 mg,3.07 mmol) in pyridine (12 mL) was added1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (735 mg,3.84 mmol) and 1-methyl-6-oxo-1,6-dihydropyridazine-3-carboxylic acid(591 mg, 3.84 mmol) and the reaction mixture stirred at room temperaturefor 22 hours. Water (25 mL) was added and the resulting precipitatecollected by filtration. The solid was dried in a vacuum oven for 1 hourand then re-dissolved in 7 N ammonia in methanol and stirred at roomtemperature for 1 hour. The solvent was then removed in vacuo to givethe title compound 702 mg (42% yield) as a yellow solid. δ_(H) NMR (500MHz, DMSO) 9.56 (s, 1H), 8.28 (d, J=2.0 Hz, 1H), 7.98 (d, J=9.7 Hz, 1H),7.92 (d, J=3.0 Hz, 1H), 7.51-7.33 (m, 2H), 7.09 (d, J=9.7 Hz, 1H), 6.84(d, J=8.8 Hz, 1H), 6.66 (dd, J=8.8, 3.0 Hz, 1H), 6.04 (ddt, J=17.2,10.5, 5.3 Hz, 1H), 5.41 (dd, J=17.3, 1.6 Hz, 1H), 5.29 (dd, J=10.5, 1.5Hz, 1H), 5.01 (s, 2H), 4.77-4.55 (m, 2H), 3.76 (s, 3H), 3.71 (s, 1H).Tr(METCR1673)=1.12 min, (ES⁺) (M+H)⁺ 409.

Step 4, Method 73:2-Methyl-6-(5-{[5-(prop-2-en-1-yloxy)pyridin-2-yl]methoxy}-1,3-benzoxazol-2-yl)-2,3-dihydropyridazin-3-one

N-(2-Hydroxy-5-{[5-(prop-2-en-1-yloxy)pyridin-2-yl]methoxy}phenyl)-1-methyl-6-oxo-1,6-dihydropyridazine-3-carboxamide(702 mg, 1.39 mmol) was suspended in acetic acid (12 mL) and heated to180° C. for 28 hours. The reaction was cooled to room temperature andconcentrated. The residue was partitioned between dichloromethane andsaturated sodium hydrogen carbonate solution, filtered and separated.The organic layer was washed with saturated sodium hydrogen carbonatesolution, dried over magnesium sulfate, and concentrated. Purificationby double recrystalisation from acetonitrile:methanol (99:1) gave thetitle compound 93 mg (17% yield) as a beige solid. Tr(METCR1673)=1.23min, (ES⁺) (M+H)⁺ 391, 83%.

Step 5, Method 73:6-{5-[(5-Hydroxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-2-methyl-2,3-dihydropyridazin-3-one

2-Methyl-6-(5-{[5-(prop-2-en-1-yloxy)pyridin-2-yl]methoxy}-1,3-benzoxazol-2-yl)-2,3-dihydropyridazin-3-one(93 mg, 0.2 mmol) and 1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)-trione (62mg, 0.4 mmol) were suspended in anhydrous N,N-dimethylformamide (3 mL)and degassed under a flow of nitrogen for 5 minutes.Tetrakis(triphenylphosphine)palladium(0) (11 mg, 0.01 mmol) was addedand the reaction stirred at room temperature under a nitrogen atmospherefor 4 hours then concentrated. The residue was triturated with water (15mL) and filtered. Purification by hot filtration from tetrahydrofuran (5mL) gave the title compound 55 mg (79% yield) as an orange powder.

Example 1, Method 73:6-{5-[(5-Hydroxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-2-methyl-2,3-dihydropyridazin-3-one

δ_(H) NMR (500 MHz, DMSO) 10.03 (s, 1H), 8.21-8.08 (m, 2H), 7.73 (d,J=8.9 Hz, 1H), 7.46 (d, J=2.5 Hz, 1H), 7.40 (d, J=8.4 Hz, 1H), 7.20 (dd,J=8.4, 2.8 Hz, 1H), 7.16-7.09 (m, 2H), 5.12 (s, 2H), 3.79 (s, 3H).Tr(MET-uHPLC-AB-101)=1.85 min, (ES⁺) (M+H)⁺ 351, 92%.

The following examples were prepared using Method 73 described above:

TABLE 74 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

350.33 6-{5-[(5- Hydroxypyridin-2- yl)methoxy]-1,3- benzoxazol-2-yl}-2-methyl-2,3- dihydropyridazin-3- one Tr(MET-uHPLC- AB-101) = 1.81 min,(ES⁺) (M + H)⁺ 351 2

376.37 5-(5-[(5- Hydroxypyridin-2- yl)methoxy]-1,3- benzoxazol-2-yl)-N-methylpyridine- 2-carboxamide Tr(MET-uHPLC- AB-101) = 2.05 min, (ES⁺)(M + H)⁺ 377Method 74

Step 1, Method 74:N-(5-bromo-2-hydroxypyridin-3-yl)-1-methyl-6-oxo-1,6-dihydropyridazine-3-carboxamide

To a solution of 1-methyl-6-oxo-1,6-dihydropyridazine-3-carboxylic acid(0.82 g, 5.34 mmol) and 3-amino-5-bromopyridin-2-ol (1.01 g, 5.34 mmol)in pyridine (20 mL) was added1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (1.54 g,8.02 mmol) and the resulting mixture stirred for 30 mins. The suspensionwas diluted with water and stood overnight. The resulting solids werefiltered, washed with water and heptane and air-dried. These solids werefurther azeotroped several times using heptane to give the titlecompound 1.53 g (88% yield) as a cream solid. δ_(H) NMR (250 MHz, DMSO)9.77 (s, 1H), 8.35 (d, J=2.6 Hz, 1H), 7.95 (d, J=9.7 Hz, 1H), 7.44 (d,J=2.6 Hz, 1H), 7.09 (d, J=9.7 Hz, 1H), 3.76 (s, 3H). Tr(MET1673)=0.98min, (ES⁺) (M+H)⁺ 325/327.

Step 2, Method 74:6-{6-Bromo-[1,3]oxazolo[5,4-b]pyridin-2-yl}-2-methyl-2,3-dihydropyridazin-3-one

A mixture of triethylamine (2.74 g, 27.07 mmol), triphenylphosphine(3.55 g, 13.53 mmol) and hexachloroethane (2.0 g, 8.46 mmol) indichloromethane (5 mL) was stirred for 10 minutes, then solidN-(5-bromo-2-hydroxypyridin-3-yl)-1-methyl-6-oxo-1,6-dihydropyridazine-3-carboxamide(1.1 g, 3.38 mmol) was added. The mixture was stirred at roomtemperature for 12 hours. The solids formed were removed by filtrationand the volatiles evaporated. Purification by FCC (silica, 2-20%tetrahydrofuran in dichloromethane), suspension in hot ethanol (circa 30mL), cooling and filtration gave the title compound 0.61 g (59% yield)as a white solid. δ_(H) NMR (500 MHz, Chloroform) 8.49 (d, J=2.1 Hz,1H), 8.24 (d, J=2.1 Hz, 1H), 8.11 (d, J=9.7 Hz, 1H), 7.09 (d, J=9.7 Hz,1H), 3.98 (s, 3H). Tr(MET1673)=1.62 min, (ES⁺) (M+H)⁺ 307/309.

Step 3, Method 74:6-{6-Hydroxy-[1,3]oxazolo[5,4-b]pyridin-2-yl}-2-methyl-2,3-dihydropyridazin-3-one

A mixture of potassium acetate (487 mg, 4.97 mmol),6-{6-bromo-[1,3]oxazolo[5,4-b]pyridin-2-yl}-2-methyl-2,3-dihydro-pyridazin-3-one(610 mg, 1.99 mmol),bis(diphenylphosphino)ferrocene]dichloropalladium(II) (145 mg, 0.2 mmol)and bis(pinacolato)diboron (554 mg, 2.18 mmol) in degassedtetrahydrofuran (15 mL) was heated to reflux for 2 hours, then cooledovernight. Water (20 mL) and ethyl acetate (20 mL) were added and theinsoluble material filtered off to give a silver grey solid. The ethylacetate layer was separated, the aqueous layer extracted with ethylacetate, the combined organic layers washed with brine (50 mL), driedover sodium sulfate and concentrated to give the boronic esterintermediate as a brown sticky solid, 0.79 g at circa 60% purity (asjudged by 1H NMR). To a solution of the boronic ester intermediateisolated above (790 mg, 1.34 mmol, 60% purity) in tetrahydrofuran (10mL) was added sodium perborate tetrahydrate (514.8 mg, 3.35 mmol) inwater (5 mL) and the resulting suspension stirred at ambient temperaturefor 2 hours. Saturated ammonium chloride solution (20 mL) and ethylacetate (20 mL) were added to the mixture and the solids removed byfiltration to give the title compound 196 mg (60% yield) as a brownsolid. δ_(H) NMR (250 MHz, DMSO) 8.13 (d, J=9.8 Hz, 1H), 7.99 (d, J=2.4Hz, 1H), 7.62 (d, J=2.4 Hz, 1H), 7.14 (d, J=9.8 Hz, 1H), 3.81 (s, 3H).Tr(MET1673)=1.30 min, (ES⁺) (M+H)⁺ 245.

Step 4, Method 74:6-{6-[(5-Methoxypyridin-2-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}-2-methyl-2,3-dihydropyridazin-3-one

To a suspension of (5-methoxypyridin-2-yl)methanol (43 mg, 0.32 mmol)and 6-{6-hydroxy-[1,3]oxazolo[5,4-b]pyridin-2-yl}-2-methyl-2,3-dihydro-pyridazin-3-one (70 mg, 0.29mmol) in toluene (5 mL) was added cyanomethylenetributylphosphorane(0.11 mL, 0.43 mmol) and the resulting mixture heated to reflux for 2hours. After cooling the volatiles were evaporated, and the residuetriturated with diethyl ether:heptane, filtered then triturated inacetonitrile:DMSO:water and filtered to give the title compound 34 mg(33% yield) as a light brown solid.

Example 1, Method 74:6-{6-[(5-Methoxypyridin-2-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}-2-methyl-2,3-dihydropyridazin-3-one

δ_(H) NMR (500 MHz, DMSO) 8.31 (d, J=2.9 Hz, 1H), 8.24 (d, J=2.7 Hz,1H), 8.15 (d, J=9.7 Hz, 1H), 8.08 (d, J=2.7 Hz, 1H), 7.56 (d, J=8.6 Hz,1H), 7.45 (dd, J=8.6, 3.0 Hz, 1H), 7.15 (d, J=9.7 Hz, 1H), 5.26 (s, 2H),3.84 (s, 3H), 3.82 (s, 3H). Tr(MET-uHPLC-AB-101)=2.2 min, (ES⁺) (M+H)⁺366.

The following examples were prepared using Method 74 described above:

TABLE 75 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

365.35 6-(6-[(5- Methoxypyridin-2- yl)methoxy]-[1,3] oxazolo[5,4-b]pyridin-2-yl}-2- methyl-2,3- dihydropyridazin- 3-one Tr(MET-uHPLC-AB-101) = 2.25 min, (ES⁺) (M + H)⁺ 366 2

397.37 6-(6-{[5-(2- Fluoroethoxy) pyridin-2-yl] methoxy}-[1,3]oxazolo[5,4-b] pyridin-2-yl)-2- methyl-2,3- dihydropyridazin- 3-oneTr(MET-uHPLC- AB-101) = 2.32 min, (ES⁺) (M + H)⁺ 398Method 75

Step 1, Method 75: 6-(Hydroxymethyl)-2-methyl-2,3-dihydropyridazin-3-one

isoButyl chloroformate (279.04 μl, 2.14 mmol) was added to a suspensionof 1-methyl-6-oxo-1,6-dihydropyridazine-3-carboxylic acid (300 mg, 1.95mmol) and triethylamine (298.43 μl, 2.14 mmol) in dry tetrahydrofuran(15 mL) at 0° C. The reaction was warmed to room temperature and stirredfor 1 hour. The mixture was concentrated in vacuo and the residuedissolved in tetrahydrofuran (15 mL). Sodium borohydride (295 mg, 7.79mmol) was added and the mixture stirred at room temperature for 1 hourthen quenched by the addition of methanol (6 mL) and water (6 mL). Themixture was extracted with dichloromethane (3×25 mL) and the combinedorganic extracts dried over magnesium sulfate, filtered andconcentrated. Purification by FCC (silica, ethyl acetate-heptane) gavethe title compound 148 mg (51% yield) as a white solid. δ_(H) NMR (500MHz, DMSO) 7.47 (d, J=9.5 Hz, 1H), 6.94 (d, J=9.5 Hz, 1H), 5.47 (t,J=6.0 Hz, 1H), 4.32 (d, J=6.0 Hz, 2H), 3.61 (s, 3H).

Step 2, Method 75:2-Methyl-6-({[2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)-2,3-dihydropyridazin-3-one

Cyanomethylenetributylphosphorane (0.18 mL, 0.7 mmol) was added to astirred solution of 2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-ol(100 mg, 0.47 mmol) and6-(hydroxymethyl)-2-methyl-2,3-dihydropyridazin-3-one (72 mg, 0.52 mmol)in toluene (3 mL) and the reaction heated to 100° C. for 20 hours undernitrogen. Cyanomethylenetributylphosphorane (0.1 mL, 0.39 mmol) and6-(hydroxymethyl)-2-methyl-2,3-dihydropyridazin-3-one (30.0 mg, 0.21mmol) were added the the mixture and heated for a further 3 hours. Thereaction was cooled to room temperature and the solid removed byfiltration and washed with toluene. Purification by triturated withdiethyl ether:heptane 1:1 (5 mL) followed by hot filtration from ethylacetate (5 mL) give the title compound 14 mg (9% yield) as a beige sold.

Example 1, Method 75:2-Methyl-6-({[2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)-2,3-dihydropyridazin-3-one

δ_(H) NMR (500 MHz, DMSO) 9.36 (d, J=1.8 Hz, 1H), 8.84 (dd, J=4.8, 1.5Hz, 1H), 8.55 (dt, J=8.0, 1.8 Hz, 1H), 8.23 (d, J=2.7 Hz, 1H), 8.11 (d,J=2.7 Hz, 1H), 7.70-7.63 (m, 2H), 7.02 (d, J=9.5 Hz, 1H), 5.15 (s, 2H),3.67 (s, 3H). Tr(MET-uHPLC-AB-101)=2.04 min, (ES⁺) (M+H)⁺ 336.

The following example was prepared using Method 75 described above:

TABLE 76 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

335.32 2-Methyl-6-({[2- (pyridin-3-yl)- [1,3]oxazolo[5,4-b]pyridin-6-yl]oxy} methyl)-2,3- dihydropyridazin- 3-one Tr(MET-uHPLC-AB-101) = 2.04 min, (ES⁺) (M + H)⁺ 336Method 76

Step 1, Method 76:N-(5-Bromo-2-chloropyridin-3-yl)pyrazine-2-carboxamide

To a solution of 5-bromo-2-chloropyridin-3-amine (5.0 g, 24.1 mmol) inpyridine (50 mL) was added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimidehydrochloride (9.24 g, 48.2 mmol) and pyrazine-2-carboxylic acid (6.58g, 53.02 mmol) and the reaction mixture stirred at room temperature for48 hours. Water (50 mL) was added and the resultant precipitatecollected by filtration to give the title compound 5.8 g (77% yield) asa beige solid. δ_(H) NMR (500 MHz, DMSO) 10.50 (s, 1H), 9.34 (d, J=1.1Hz, 1H), 9.01 (d, J=2.5 Hz, 1H), 8.91-8.83 (m, 1H), 8.78 (d, J=2.3 Hz,1H), 8.45 (d, J=2.1 Hz, 1H) Tr(METCR1673)=1.32 min, (ES⁺) (M+H)⁺313/315.

Step 2, Method 76: 2-{6-Bromo-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyrazine

To a solution of N-(5-bromo-2-chloropyridin-3-yl)pyrazine-2-carboxamide(4.79 g, 15.28 mmol) in N,N-dimethylacetamide (100 mL) was addedpotassium phosphate (3.242 g, 15.28 mmol) and the resulting mixture wasstirred at 180° C. for 4.5 hours. The reaction mixture was cooled toroom temperature and filtered. The filtrate was concentrated, the solidtriturated with water. Purification by FCC (silica, 0-100% ethyl acetatein heptane) gave the title compound 1.72 g (35% yield) as an orangesolid. δ_(H) NMR (500 MHz, DMSO) 9.51 (s, 1H), 8.92 (s, 2H), 8.74 (d,J=2.1 Hz, 1H), 8.62 (d, J=2.1 Hz, 1H)) Tr(METCR1673)=1.08 min, (ES⁺)(M+H)⁺ 277/279, 88%.

Step 3, Method 76:2-[6-(Tetramethyl-1,3,2-dioxaborolan-2-yl)-[1,3]oxazolo[5,4-b]pyridin-2-yl]pyrazine

A solution of 2-{6-bromo-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyrazine (625mg, 2.26 mmol), bis(pinacolato)diboron (630 mg, 2.48 mmol) and potassiumacetate (0.55 g, 5.64 mmol) in tetrahydrofuran (31 mL) was degassed withnitrogen for 5 minutes.Bis(diphenylphosphino)ferrocene]dichloropalladium(II) (0.17 g, 0.23mmol) was added and the reaction was stirred at 70° C. for 20 hours. Themixture was cooled to room temperature, diluted with water (100 mL) andfiltered. The filtrate was extracted with ethyl acetate (3×100 mL), theorganic layers combined, dried over magnesium sulfate, filtered andconcentrated to give the title compound 1.11 g (88% yield) as a brownoil Tr(METCR1673)=0.78 min, (ES⁺) (M+H)⁺ 242 mass of boronic acid, 58%.

Step 4, Method 76: 2-(Pyrazin-2-yl)-[1,3]oxazolo[5,4-b]pyridin-6-ol

2-[6-(Tetramethyl-1,3,2-dioxaborolan-2-yl)-[1,3]oxazolo[5,4-b]pyridin-2-yl]pyrazine(1.11 g, 2.05 mmol) was dissolved in 1:1 tetrahydrofuran-water (30 mL).Sodium perborate tetrahydrate (790 mg, 5.14 mmol) was added and themixture stirred at room temperature for 24 hours. Saturated ammoniumchloride solution (60 mL) was added and the product extracted with ethylacetate (3×100 mL). The organic layers were combined, dried overmagnesium sulfate, filtered and concentrated. Trituration with diethylether gave the title compound 244 mg (52% yield) as a brown solid. δ_(H)NMR (500 MHz, DMSO) 10.28 (s, 1H), 9.47 (d, J=1.3 Hz, 1H), 9.02-8.76 (m,2H), 8.03 (d, J=2.6 Hz, 1H), 7.68 (d, J=2.6 Hz, 1H) Tr(METCR1673)=0.80min, (ES⁺) (M+H)⁺ 215, 94%.

Step 5, Method 76:2-{6-[(5-Methoxypyridin-2-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyrazine

2-(Pyrazin-2-yl)-[1,3]oxazolo[5,4-b]pyridin-6-ol (150 mg, 0.66 mmol) and(5-methoxypyridin-2-yl) methanol (101 mg, 0.72 mmol) were suspended inanhydrous toluene (4 mL), cyanomethylenetributylphosphorane (0.26 mL,0.99 mmol) added and the reaction heated to 100° C. in a sealed tube for7 hours. The reaction mixture was cooled to room temperature and thesolvents removed. The residue was triturated with 1:1 diethyl ether:heptane (10 mL). Purification by recrystalisation from tetrahydrofurangave the title compound 41 mg (18% yield) as a beige solid.

Example 1, Method 76:2-{6-[(5-Methoxypyridin-2-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyrazine

δ_(H) NMR (500 MHz, DMSO) 9.49 (d, J=1.1 Hz, 1H), 8.99-8.79 (m, 2H),8.31 (d, J=2.9 Hz, 1H), 8.28 (d, J=2.7 Hz, 1H), 8.13 (d, J=2.7 Hz, 1H),7.57 (d, J=8.6 Hz, 1H), 7.45 (dd, J=8.6, 2.9 Hz, 1H), 5.28 (s, 2H), 3.84(s, 3H). Tr(MET-uHPLC-AB-101)=2.21 min, (ES⁺) (M+H)⁺ 336.

The following examples were prepared using Method 76 described above:

TABLE 77 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

335.32 2-{6-[(5- Methoxypyridin-2- yl)methoxy]- [1,3]oxazolo[5,4-b]pyridin-2-yl} pyrazine Tr(MET-uHPLC- AB-101) = 2.21 min, (ES⁺) (M + H)⁺336 2

338.33 2-Methoxy-5-({[2- (1-methyl-1H- pyrazol-4-yl)-[1,3]oxazolo[5,4-b] pyridin-6-yl]oxy} methyl) pyrazine Tr(MET-uHPLC-AB-101) = 2.51 min, (ES⁺) (M + H)⁺ 339Method 77

Step 1, Method 77: Methyl 5-(carbonochloridoyl)pyridine-2-carboxylate

Thionyl chloride (0.47 mL, 5.52 mmol) was added to6-(methoxycarbonyl)pyridine-3-carboxylic acid (500 mg, 2.76 mmol) intoluene (5.0 mL) and dichloromethane (2.5 mL), followed byN,N-dimethylformamide (2 drops). After gas evolution had ceased thereaction was heated to 60° C. under nitrogen for 4 hours. The reactionwas cooled to room temperature and concentrated in vacuo, dissolved intoluene (30 mL) and re-concentrated in vacuo. The solid was dried undervacuum for 1 hour to give the title compound 0.52 g (95% yield) as anoff white solid. This material was used in the next step without furtherpurification.

Step 2, Method 77: Methyl5-[(5-bromo-2-chloropyridin-3-yl)carbamoyl]pyridine-2-carboxylate

Methyl 5-(carbonochloridoyl)pyridine-2-carboxylate (3.86 g, 19.34 mmol)was added to 5-bromo-2-chloropyridin-3-amine (4.01 g, 19.34 mmol) inpyridine (80 mL) and the reaction mixture stirred at room temperatureovernight. Water (80 mL) was added and the mixture stirred for a further30 minutes. The precipitate was filtered, washed with water and dried ina vacuum oven to give the title compound 7.16 g (69% yield) as a whitesolid. δ_(H) NMR (500 MHz, DMSO) 10.78 (s, 1H), 9.21 (d, J=1.6 Hz, 1H),8.53 (d, J=2.3 Hz, 1H), 8.49 (dd, J=8.1, 2.2 Hz, 1H), 8.44 (d, J=2.3 Hz,1H), 8.23 (dd, J=8.1, 0.6 Hz, 1H), 3.93 (s, 3H), Tr(METCR1410)=1.01 min,(ES⁺) (M+H)⁺ 370/372/374.

Step 3, Method 77:5-{6-Bromo-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine-2-carboxylic acid

Potassium phosphate (207 mg, 0.98 mmol) was added to methyl5-[(5-bromo-2-chloropyridin-3-yl)carbamoyl]pyridine-2-carboxylate (0.36g, 0.98 mmol) in N,N-dimethylacetamide (12 mL) and the mixture stirredat 180° C. overnight. The reaction was cooled to room temperature andfiltered. The solid was washed with water and dried in a vacuum oven togive the title compound 0.286 g (91% yield) as an off white solid. δ_(H)NMR (250 MHz, DMSO) 9.41 (d, J=1.6 Hz, 1H), 8.72 (dd, J=8.3, 2.2 Hz,1H), 8.64 (d, J=2.1 Hz, 1H), 8.54 (d, J=2.1 Hz, 1H), 8.25 (d, J=8.2 Hz,1H). Tr(METCR1673)=1.08 min, (ES⁺) (M+H)⁺ 320/322.

Step 4, Method 77: Methyl5-{6-bromo-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine-2-carboxylate

Thionyl dichloride (170 μl, 0 mol) was added to5-{6-bromo-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine-2-carboxylic acid(1.5 g, 5.0 mmol) in methanol (25 mL) and the reaction heated to refluxunder nitrogen for 17 hours. The reaction was cooled to room temperatureand the solid filtered, washed with methanol (20 mL) and dried in avacuum oven to give the title compound 0.81 g (43.4% yield) as an offwhite solid. Tr(METCR1410)=1.07 min, (ES⁺) (M+H)⁺ 334/336, 84%.

Step 5, Method 77: Methyl5-[6-(tetramethyl-1,3,2-dioxaborolan-2-yl)-[1,3]oxazolo[5,4-b]pyridin-2-yl]pyridine-2-carboxylate

Methyl 5-{6-bromo-[1,3]oxazolo[4,5-b]pyridin-2-yl}pyridine-2-carboxylate(800 mg, 2.39 mmol), bis(pinacolato)diboron (912 mg, 3.59 mmol) andpotassium acetate (940 mg, 9.58 mmol) were dissolved in tetrahydrofuran(30 mL) and de-gassed with nitrogen. To this was addedbis(diphenylphosphino)ferrocene]dichloropalladium(II) (175 mg, 0.24mmol) and the reaction heated to 80° C. for 2 hours. The reaction wascooled to room temperature and filtered. The organic layer wasconcentrated in vacuo and the solid sonicated in diethyl ether:heptane(1:1). Filtration to give the title compound 0.793 g (74% yield) as alight brown solid. This material was used in the next step withoutfurther purification.

Step 6, Method 77: Methyl5-{6-hydroxy-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine-2-carboxylate

Sodium perborate tetrahydrate (38 mg, 0.25 mmol) was added to methyl5-[6-(tetramethyl-1,3,2-dioxaborolan-2-yl)-[1,3]oxazolo[5,4-b]pyridin-2-yl]pyridine-2-carboxylate(62%, 152 mg, 0.25 mmol) in tetrahydrofuran (5 mL) and water (2.5 mL)and the reaction stirred at room temperature for 1.5 hours. Saturatedammonium chloride solution (5 mL) was added and the aqueous layerextracted with ethyl acetate (3×25 mL). The combined organic layers weredried over sodium sulfate and concentrated. Purification by FCC (0-100%tetrahydrofuran in heptane) gave the title compound 44 mg (58% yield) asan off white solid. δ_(H) NMR (500 MHz, DMSO) 10.23 (s, 1H), 9.45 (dd,J=2.2, 0.7 Hz, 1H), 8.71 (dd, J=8.2, 2.2 Hz, 1H), 8.27 (dd, J=8.2, 0.7Hz, 1H), 8.01 (d, J=2.6 Hz, 1H), 7.67 (d, J=2.6 Hz, 1H), 3.95 (d, J=3.4Hz, 3H), Tr(METCR1410)=0.89 min, (ES⁺) (M+H)⁺ 272, 89%.

Step 7, Method 77: Methyl5-{6-[(5-methoxypyridin-2-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine-2-carboxylate

Cyanomethylenetributylphosphorane (0.31 mL, 1.19 mmol) was added to astirred solution of methyl5-{6-hydroxy-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine-2-carboxylate (215mg, 0.79 mmol) and (5-methoxypyridin-2-yl)methanol (132 mg, 0.95 mmol)in toluene (5 mL) and the reaction heated to 100° C. for 3.5 hours undernitrogen. The reaction was cooled to room temperature and the solidfiltered. The solid was washed with toluene (15 mL) and dried in a vacoven to give the title compound 216 mg (62% yield) as a beige solid.δ_(H) NMR (500 MHz, DMSO) 9.42 (d, J=1.6 Hz, 1H), 8.72 (dd, J=8.2, 2.2Hz, 1H), 8.66 (d, J=2.8 Hz, 1H), 8.31 (d, J=2.7 Hz, 1H), 8.27 (d, J=7.9Hz, 1H), 8.22 (dd, J=8.9, 2.8 Hz, 1H), 8.19 (d, J=2.7 Hz, 1H), 8.14 (d,J=9.0 Hz, 1H), 5.60 (s, 2H), 3.98 (s, 3H), 3.91 (s, 3H),Tr(METCR1410)=1.02 min, (ES⁺) (M+H)⁺ 393, 89%.

Step 8, Method 77:5-{6-[(5-Methoxypyridin-2-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine-2-carboxylicacid

2 M sodium hydroxide (0.08 mL) was added to a solution of methyl5-{6-[(5-methoxypyridin-2-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine-2-carboxylate(50 mg, 0.12 mmol) in tetrahydrofuran (1 mL) and the reaction stirred atroom temperature overnight. Additional 2 M sodium hydroxide (0.05 mL)and tetrahydrofuran (1 mL) were added and the reaction stirred for afurther 5 hours. The reaction was filtered under reduced pressure andthe solid washed with water (5 mL) and dried under vacuum to give thesodium salt. The solid was suspended in water (2 mL) and 4 Nhydrochloric acid in dioxane (0.2 mL) was added. The solid was sonicateduntil the solid became a fine powder and then concentrated in vacuo togive the title compound 52 mg (80% yield) as a light yellow solid.Tr(METCR1410)=0.94 min, (ES⁺) (M+H)⁺ 379, 80%.

Step 9, Method 77:5-{6-[(5-Methoxypyridin-2-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}-N-methylpyridine-2-carboxamide

Diisopropylethylamine (20 μl, 0.12 mmol) was added to5-{16-[(5-Methoxypyridin-2-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine-2-carboxylicacid hydrochloride (80%, 52 mg, 0.1 mmol),1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium3-oxid hexafluorophosphate (46.9 mg, 0.12 mmol) and methanaminehydrochloride (1:1) (8 mg, 0.12 mmol) suspended in N,N-dimethylformamide(2 mL) and the reaction stirred at room temperature for 2 hours. Thesolid was filtered and washed with N,N-dimethylformamide (10 mL). Thesample was triturated with methanol (3 mL) and then tetrahydrofuran (3mL). The product was purified by re-crystallisation from DMSO (2 mL)followed by washing with DMSO (3 mL), water (5 mL) and methanol (5 mL).The solid was dried in a vacuum oven overnight to give the titlecompound 12 mg (29% yield) as an off white solid.

Example 1, Method 77:5-{6-[(5-Methoxypyridin-2-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}-N-methylpyridine-2-carboxamide

δ_(H) NMR (500 MHz, Pyridine) 9.51 (s, 1H), 9.30 (d, J=4.0 Hz, 1H), 8.64(dd, J=8.1, 1.8 Hz, 1H), 8.58-8.49 (m, 3H), 8.15 (d, J=2.5 Hz, 1H),7.64-7.61 (m, 1H), 7.35 (dd, J=8.6, 2.9 Hz, 1H), 5.47 (s, 2H), 3.73 (s,3H), 3.13 (d, J=4.9 Hz, 3H), Tr(MET-uHPLC-AB-101)=2.51 min, (ES⁺) (M+H)⁺392.

The following example was prepared using Method 77 described above:

TABLE 78 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

391.39 5-{6-[(5- Methoxypyridin-2- yl)methoxy]- [1,3]oxazolo[5,4-b]pyridin-2-yl}-N- methylpyridine-2- carboxamide Tr(MET-uHPLC- AB-101) =2.51 min, (ES⁺) (M + H)⁺ 392Method 78

Step 1, Method 78:N-{2-Hydroxy-5-[(5-methoxypyridin-2-yl)methoxy]phenyl}-4-methyl-5-oxo-4,5-dihydropyrazine-2-carboxamide

2-Amino-4-[(5-methoxypyridin-2-yl)methoxy]phenol dihydrochloride (95%,200 mg, 0.6 mmol, prepared using Method 33) and4-methyl-5-oxo-4,5-dihydropyrazine-2-carbonyl chloride (50%, 226 mg,0.65 mmol) were suspended in pyridine (5 mL) and the reaction stirred atroom temperature in a nitrogen atmosphere for 2 hours. The reaction wasconcentrated in vacuo and triturated with water (20 mL). The mixture wasfiltered through glass fibre filter paper and dried in air overnight togive the title compound 203 mg (71% purity, 63% yield) as a yellowpowder. δ_(H) NMR (500 MHz, DMSO) 9.82 (d, J=1.5 Hz, 1H), 8.55 (s, 1H),8.28 (d, J=2.9 Hz, 1H), 8.08 (d, J=3.0 Hz, 1H), 8.06 (d, J=0.9 Hz, 1H),7.47 (d, J=8.6 Hz, 1H), 7.43 (dd, J=8.6, 2.9 Hz, 1H), 6.83 (d, J=8.7 Hz,1H), 6.62 (dd, J=8.8, 3.0 Hz, 1H), 5.02 (s, 2H), 3.84 (s, 4H), 3.55 (s,3H). Tr(METCR1410)=0.88 min, (ES⁺) (M+H)⁺ 383, 71%.

Step 2, Method 78:5-{5-[(5-Methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-1-methyl-1,2-dihydropyrazin-2-one

N-{2-Hydroxy-5-[(5-methoxypyridin-2-yl)methoxy]phenyl}-4-methyl-5-oxo-4,5-dihydropyrazine-2-carboxamide(71%, 203 mg, 0.38 mmol) was suspended in acetic acid (2 mL) and heatedto 180° C. in a sealed tube for 16 hours. The solvents were removed invacuo and the residue partitioned between ethyl acetate (30 mL) andsaturated sodium bicarbonate solution (10 mL). The aqueous was extractedwith ethyl acetate (2×30 mL), the combined organics washed with brine(10 mL), dried over anhydrous magnesium sulfate, filtered andconcentrated. Purification by FCC (silica, 0-10% methanol indichloromethane), trituration with diethyl ether, hot filtration fromDMSO, preparative HPLC (acetonitrile/water and acetonitrile/water+0.2%ammonium hydroxide) gave the title compound, 4 mg (3% yield) as a whitepowder.

Example 1, Method 78:5-{5-[(5-Methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-1-methyl-1,2-dihydropyrazin-2-one

δ_(H) NMR (500 MHz, DMSO) 8.78 (s, 1H), 8.30 (d, J=2.9 Hz, 1H), 8.13 (d,J=0.9 Hz, 1H), 7.65 (d, J=8.9 Hz, 1H), 7.52 (d, J=8.6 Hz, 1H), 7.43 (dd,J=8.6, 3.0 Hz, 1H), 7.37 (d, J=2.5 Hz, 1H), 7.07 (dd, J=8.9, 2.5 Hz,1H), 5.17 (s, 2H), 3.84 (s, 3H), 3.57 (s, 3H). Tr(MET-uHPLC-AB-101)=2.11min, (ES⁺) (M+H)⁺ 365.

The following example was prepared using Method 78 described above:

TABLE 79 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

364.36 5-{5-[(5- Methoxypyridin-2- yl)methoxy]-1,3- benzoxazol-2-yl}-1-methyl-1,2- dihydropyrazin-2- one Tr(MET-uHPLC- AB-101) = 2.11 min,(ES⁺) (M + H)⁺ 365Method 79

Step 1, Method 79:5-Methoxy-2-({[2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)pyridin-1-ium-1-olateand3-{6-[(5-methoxy-1-oxidopyridin-1-ium-2-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridin-1-ium-1-olate

3-{6-[(5-Methoxypyridin-2-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine(93%, 78 mg, 0.22 mmol, prepared using Method 30) was dissolved inanhydrous dichloromethane (2 mL), 3-chlorobenzenecarboperoxoic acid(75%, 55 mg, 0.24 mmol) was added and the reaction stirred at roomtemperature for 2 hours. 3-Chlorobenzenecarboperoxoic acid (75%, 55 mg,0.24 mmol) was added and the reaction stirred at room temperature for 16hours. The reaction was diluted with dichloromethane (50 mL) and theorganic layer washed with saturated sodium hydrogen carbonate solution(3×30 mL), saturated sodium sulfite solution (30 mL), dried overmagnesium sulfate, filtered and concentrated. Purification bypreparative HPLC (acetonitrile/water) gave the two title compounds5-methoxy-2-({[2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)pyridin-1-ium-1-olate8.1 mg (11% yield) as a white powder and3-{6-[(5-methoxy-1-oxidopyridin-1-ium-2-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridin-1-ium-1-olate6.2 mg (8% yield) as a white powder.

Example 1, Method 79:5-Methoxy-2-({[2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)pyridin-1-ium-1-olate

δ_(H) NMR (500 MHz, DMSO) 9.36 (d, J=1.6 Hz, 1H), 8.84 (dd, J=4.8, 1.6Hz, 1H), 8.55 (dt, J=8.0, 1.9 Hz, 1H), 8.25 (d, J=2.7 Hz, 1H), 8.22 (d,J=2.3 Hz, 1H), 8.12 (d, J=2.7 Hz, 1H), 7.71-7.64 (m, 1H), 7.62 (d, J=8.9Hz, 1H), 7.12 (dd, J=8.9, 2.4 Hz, 1H), 5.36 (s, 2H), 3.84 (s, 3H).Tr(MET-uHPLC-AB-101)=1.99 min, (ES⁺) (M+H)⁺ 351.

Example 2, Method 79:3-{6-[(5-Methoxy-1-oxidopyridin-1-ium-2-yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridin-1-ium-1-olate

δ_(H) NMR (500 MHz, DMSO) 8.80 (s, 1H), 8.46 (d, J=7.2 Hz, 1H), 8.29 (d,J=2.7 Hz, 1H), 8.22 (d, J=2.3 Hz, 1H), 8.15 (d, J=2.7 Hz, 1H), 8.06 (d,J=8.1 Hz, 1H), 7.69-7.63 (m, 1H), 7.62 (d, J=8.9 Hz, 1H), 7.11 (dd,J=8.9, 2.3 Hz, 1H), 5.36 (s, 2H), 3.84 (s, 3H).Tr(MET-uHPLC-AB-101)=1.58 min, (ES⁺) (M+H)⁺ 367.

The following examples were prepared using Method 79 described above:

TABLE 80 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

350.33 5-Methoxy-2-({[2- (pyridin-3-yl)- [1,3]oxazolo[5,4-b]pyridin-6-yloxy} methyl)pyridin-1- ium-1-olate Tr(MET-uHPLC- AB-101) =1.99 min, (ES⁺) (M + H)⁺ 351 2

366.33 3-(6-[(5-Methoxy- 1-oxidopyridin-1- ium-2-yl)methoxy]-[1,3]oxazolo[5,4-b] pyridin-2-yl}pyridin- 1-ium-1-olate Tr(MET-uHPLC-AB-101) = 1.58 min, (ES⁺) (M + H)⁺ 367Method 80

Step 1, Method 80: Methyl 6-(methylcarbamoyl)pyridine-3-carboxylate

5-(Methoxycarbonyl)pyridine-2-carboxylic acid (1 g, 5.52 mmol) wassuspended in thionyl chloride (10 mL, 137.02 mmol), anhydrousN,N-dimethylformamide (0.01 mL) was added and the reaction heated to 80°C. under a nitrogen atmosphere for 1 hour. The reaction mixture wascooled to room temperature and the solvents removed in vacuo. The solidwas dissolved in anhydrous tetrahydrofuran (25 mL) and stirred under anitrogen atmosphere. 2 M methylamine in tetrahydrofuran (8.28 mL) wasadded dropwise and the reaction was stirred at 50° C. for 2 hours. Thereaction was cooled to room temperature and the volatiles removed invacuo. The residue was triturated with water and filtered to give thetitle compound 765 mg (71% yield) as a beige powder. Tr(METCR1410)=0.81min, (ES⁺) (M+H)⁺ 195.

Step 2, Method 80:5-(Methoxycarbonyl)-2-(methylcarbamoyl)pyridin-1-ium-1-olate

Methyl 6-(methylcarbamoyl)pyridine-3-carboxylate (700 mg, 3.6 mmol) wassuspended in anhydrous dichloromethane (20 mL),3-chlorobenzenecarboperoxoic acid (1.74 g, 7.58 mmol) was added and thereaction was stirred at 45° C. for 3.5 days under a nitrogen atmosphere.The reaction was cooled to room temperature and diluted withdichloromethane (100 mL). The organic extract was washed with saturatedsodium hydrogen carbonate solution (3×30 mL), saturated sodium sulfitesolution solution (30 mL) then dried over anhydrous sodium sulfate,filtered and concentrated. The residue was dissolved in dichloromethane(30 mL) and washed with sodium hydrogen carbonate solution (3×15 mL).The organic layer was dried over magnesium sulfate, filtered andconcentrated in vacuo. This solid was dissolved in dichloromethane (30mL) and washed with sodium hydrogen carbonate solution (3×15 mL). Theorganic layer was dried over magnesium sulfate, filtered andconcentrated in vacuo. Purification by FCC (silica, 0-10% methanol indichloromethane) gave the title compound 425 mg (53% yield) as a whitesolid. Tr(METCR1410)=0.69 min, (ES⁺) (M+H)⁺ 211.

Step 3, Method 80: 5-Carboxy-2-(methylcarbamoyl)pyridin-1-ium-1-olate

5-(Methoxycarbonyl)-2-(methylcarbamoyl)pyridin-1-ium-1-olate (95%, 425mg, 1.98 mmol) was suspended in tetrahydrofuran (10 mL), 2 M sodiumhydroxide (0.96 mL) was added and the reaction mixture stirred at roomtemperature for 1.5 hours. The reaction mixture was acidified to pH 3using 1 M hydrochloric acid and a gummy solid formed. Water was added tothe mixture and the solid dissolved. The aqueous was extracted withethyl acetate and the organic layer was concentrated. Purification bypreparative HPLC (acetonitrile/water) gave the title compound 57 mg (15%yield) as a white solid. Tr(METCR1410)=0.30 min, (ES⁺) (M+H)⁺ 197.

Step 4, Method 80:5-({2-Hydroxy-5-[(5-methoxypyridin-2-yl)methoxy]phenyl}carbamoyl)-2-(methylcarbamoyl)pyridin-1-ium-1-olate

2-Amino-4-[(5-methoxypyridin-2-yl)methoxy]phenol (41 mg, 0.13 mmol,prepared using Method 33) and5-carboxy-2-(methylcarbamoyl)pyridin-1-ium-1-olate (25 mg, 0.13 mmol)were dissolved in pyridine (1 mL) and stirred at room temperature for 10minutes. 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (29mg, 0.15 mmol) was added and the reaction mixture was left to stir atroom temperature for 2 hours. Water was added to the reaction mixtureand filtered. Purification by FCC (silica, 0-100% ethyl acetate inheptane followed by 0-20% methanol in dichloromethane) gave the titlecompound 12 mg (22% yield) as a yellow solid. δ_(H) NMR (500 MHz, DMSO)10.89 (d, J=4.8 Hz, 1H), 9.97 (s, 1H), 9.26 (s, 1H), 8.89 (s, 1H), 8.32(d, J=8.4 Hz, 1H), 8.27 (d, J=2.4 Hz, 1H), 8.00 (d, J=7.8 Hz, 1H), 7.46(d, J=8.5 Hz, 1H), 7.41 (dd, J=8.6, 2.9 Hz, 1H), 7.33 (d, J=2.7 Hz, 1H),6.83 (d, J=8.8 Hz, 1H), 6.76 (dd, J=8.9, 3.0 Hz, 1H), 5.01 (s, 2H), 3.83(s, 3H), 2.92 (d, J=4.9 Hz, 3H). Tr(MET-uHPLC-AB-101)=1.75 min, (ES⁺)(M+H)⁺ 425.

Step 5, Method 80:5-{5-[(5-Methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-2-(methylcarbamoyl)pyridin-1-ium-1-olate

5-({2-Hydroxy-5-[(5-methoxypyridin-2-yl)methoxy]phenyl}carbamoyl)-2-(methylcarbamoyl)pyridin-1-ium-1-olate(102 mg, 0.24 mmol) was suspended in acetic acid (4 mL) andpara-toluenesulfonic acid (457 mg, 2.4 mmol) added. The mixture wasirradiated in the microwave at 120° C. for 2 hours. The mixture wascooled to room temperature and the pH adjusted to 7 by addition ofsaturated sodium bicarbonate solution. The product was extracted withethyl acetate (3×50 mL), dried over magnesium sulfate and concentrated.Purification by FCC (Silica, 0-10% methanol in dichloromethane), andpreparative HPLC (acetonitrile/water+0.2% ammonium hydroxide) gave thetitle compound 5.4 mg (6%) as a white powder.

Example 1, Method 80:5-{5-[(5-Methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}-2-(methylcarbamoyl)pyridin-1-ium-1-olate

δ_(H) NMR (500 MHz, DMSO) 10.78 (q, J=4.9 Hz, 1H), 8.95 (s, 1H), 8.39(d, J=8.4 Hz, 1H), 8.30 (d, J=2.9 Hz, 1H), 8.22 (dd, J=8.4, 1.3 Hz, 1H),7.77 (d, J=9.0 Hz, 1H), 7.56-7.50 (m, 2H), 7.43 (dd, J=8.6, 3.0 Hz, 1H),7.20 (dd, J=9.0, 2.5 Hz, 1H), 5.20 (s, 2H), 3.84 (s, 3H), 2.92 (d, J=4.9Hz, 3H). Tr(MET-uHPLC-AB-101)=2.4 min, (ES⁺) (M+H)⁺ 407.

The following example was prepared using Method 80 described above:

TABLE 81 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

406.40 5-{5-[(5- Methoxypyridin-2- yl)methoxy]-1,3- benzoxazol-2-yl)-2-(methylcarbamoyl) pyridin-1-ium-1-olate Tr(MET-uHPLC- AB-101) = 2.4 min,(ES⁺) (M + H)⁺ 407Method 81

Step 1, Method 81: [5-(Prop-2-en-1-yloxy)pyridin-2-yl]methylN-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]carbamate

2-(Pyridin-3-yl)-1,3-benzoxazol-5-amine (500 mg, 2.37 mmol) wasdissolved in tetrahydrofuran (40 mL) and triphosgene (232 mg, 0.78 mmol)added. The solution was stirred at room temperature for 10 minutes undera nitrogen flow attached to a 2 M sodium hydroxide scrubber.Triethylamine (0.51 mL, 3.55 mmol) was added and the reaction mixtureleft to stir for a further 30 minutes.[5-(Prop-2-en-1-yloxy)pyridin-2-yl]methanol (391 mg, 2.37 mmol,described in in U.S. Pat. No. 4,198,416 (1978) reference example 3) wasdissolved in tetrahydrofuran (6 mL) and passed through magnesium sulfateunder nitrogen into the top of a closed dropping funnel, the magnesiumsulfate was washed with tetrahydrofuran into the dropping funnel undernitrogen. The dried allyl alcohol was added dropwise to the reactionmixture. The reaction mixture was stirred for 2 days at roomtemperature. The solvents were removed in vacuo, the residue trituratedwith water (50 mL) and filtered. The solid was suspended in 4:1tetrahydrofuran:dichloromethane and heated to 50° C. The hot mixture wasfiltered and filtrate was concentrated in vacuo. The remaining residuewas triturated in 1:1 diethyl ether:heptane to give the title compound165 mg (15% yield) as a brown solid. δ_(H) NMR (500 MHz, DMSO) 10.02 (s,1H), 9.33 (d, J=1.6 Hz, 1H), 8.80 (dd, J=4.8, 1.6 Hz, 1H), 8.52 (dt,J=8.0, 1.9 Hz, 1H), 8.30 (t, J=1.8 Hz, 1H), 8.00 (s, 1H), 7.75 (d, J=8.8Hz, 1H), 7.65 (dd, J=8.6, 4.9 Hz, 1H), 7.49 (dd, J=8.8, 2.0 Hz, 1H),7.45 (d, J=1.8 Hz, 2H), 6.04 (ddt, J=17.3, 10.5, 5.3 Hz, 1H), 5.41 (dq,J=17.3, 1.6 Hz, 1H), 5.35-5.24 (m, 1H), 5.18 (s, 2H), 4.67 (dt, J=5.2,1.5 Hz, 2H); Tr(METCR1410)=1.08 min, (ES⁺) (M+H)⁺ 403, 84%.

Step 2, Method 81: (5-Hydroxypyridin-2-yl)methylN-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]carbamate

5[5-(Prop-2-en-1-yloxy)pyridin-2-yl]methylN-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]carbamate (84%, 145 mg, 0.3mmol) and 1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)-trione (95 mg, 0.61mmol) were suspended in N,N-dimethylformamide (4 mL) and degassed undera flow of nitrogen. Tetrakis(triphenylphosphine)palladium(0) (17 mg,0.02 mmol) was added and the reaction mixture stirred at roomtemperature for 1.5 hours. The reaction mixture was concentrated to ¼ ofthe original volume and water added. A precipitate formed which wascollected by filtration. The collected solid was triturated with ethylacetate and purified by a hot filtration from acetonitrile to give thetitle compound 57 mg (50% yield) as an orange solid.

Example 1, Method 81: (5-Hydroxypyridin-2-yl)methylN-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]carbamate

δ_(H) NMR (500 MHz, DMSO) 10.08-9.92 (m, 2H), 9.33 (d, J=1.7 Hz, 1H),8.80 (dd, J=4.8, 1.6 Hz, 1H), 8.52 (dt, J=8.0, 1.9 Hz, 1H), 8.12 (d,J=2.8 Hz, 1H), 8.00 (s, 1H), 7.74 (d, J=8.8 Hz, 1H), 7.65 (ddd, 1H),7.49 (dd, J=8.9, 1.9 Hz, 1H), 7.34 (d, J=8.4 Hz, 1H), 7.20 (dd, J=8.4,2.9 Hz, 1H), 5.13 (s, 2H). Tr(MET-uHPLC-AB-101)=1.82 min, (ES⁺) (M+H)⁺363.

The following example was prepared using Method 81 described above:

TABLE 82 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

362.35 (5-Hydroxypyridin- 2-yl)methyl N-[2- (pyridin-3-yl)-1,3-benzoxazol-5- yl]carbamate Tr(MET-uHPLC- AB-101) = 1.82 min, (ES⁺) (M +H)⁺ 363Method 82

Step 1, Method 82:N-(2-Hydroxy-5-nitrophenyl)-1-methyl-6-oxo-1,6-dihydropyridazine-3-carboxamide

To a suspension of 2-amino-4-nitrophenol (3.0 g, 19.46 mmol) and1-methyl-6-oxo-1,6-dihydropyridazine-3-carboxylic acid (3.06 g, 19.85mmol) in pyridine (30 mL) was added1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (4.85 g,25.3 mmol) and the resulting suspension was stirred for 1 hour. Thereaction mixture was slowly diluted with water (circa 70 mL) and thesuspension stirred for 5 minutes. The solids were filtered off andair-dried to give the title compound 4.67 g (74% yield) as a tan solid.δ_(H) NMR (250 MHz, DMSO) 9.67 (s, 1H), 9.10 (d, J=2.8 Hz, 1H),8.06-7.93 (m, 2H), 7.12 (dd, J=9.3, 3.8 Hz, 2H), 3.79 (s, 3H). Contains14 wt % pyridine. Tr(METCR1410, 2 min)=1.03 min (ES⁺) (M+H)⁺ 291.

Step 2, Method 82:2-Methyl-6-(5-nitro-1,3-benzoxazol-2-yl)-2,3-dihydropyridazin-3-one

Polyphosphoric acid (approximately 20 mL) was poured ontoN-(2-hydroxy-5-nitrophenyl)-1-methyl-6-oxo-1,6-dihydropyridazine-3-carboxamide(90%, 4.67 g, 14.48 mmol). The lumps were broken up and the resultingsuspension heated to 110° C. for 3 hours. The mixture was cooled and thedeep red solution added to ice-water (100 mL). The mixture was dilutedwith more water to give a total volume of circa 200 mL. A thick purplesuspension resulted, to which ethyl acetate was added (circa 50 mL) andthe suspension stirred rapidly for 15 mins. A tan solid formed which wasremoved by filtration. These solids were washed with water, heptane andair-dried under vacuum to give the title compound 2.95 g (75% yield) asa grey solid. δ_(H) NMR (250 MHz, DMSO) 8.74 (d, J=2.2 Hz, 1H), 8.41(dd, J=9.0, 2.3 Hz, 1H), 8.19 (d, J=9.7 Hz, 1H), 8.13 (d, J=9.0 Hz, 1H),7.18 (d, J=9.7 Hz, 1H), 3.83 (s, 3H). Tr(METCR0990)=1.48 min (ES⁺)(M+H)⁺ 273, 93%.

Step 3, Method 82:6-(5-Amino-1,3-benzoxazol-2-yl)-2-methyl-2,3-dihydropyridazin-3-one

A suspension of2-methyl-6-(5-nitro-1,3-benzoxazol-2-yl)-2,3-dihydropyridazin-3-one(95%, 2.45 g, 8.55 mmol) in ethanol: N,N-dimethylformamide (1:1, 100 mL)and 10% palladium on carbon (0.45 g) was stirred under an atmosphere ofhydrogen for 4 hours. The mixture was filtered, washed withN,N-dimethylformamide. The filtrates were evaporated to give the titlecompound (2.1 g, 92% yield) as a green to yellow solid. 6H NMR (250 MHz,DMSO) 8.11 (d, J=9.7 Hz, 1H), 7.46 (d, J=8.7 Hz, 1H), 7.11 (d, J=9.7 Hz,1H), 6.89 (d, J=1.9 Hz, 1H), 6.73 (dd, J=8.7, 2.2 Hz, 1H), 5.22 (s, 2H),3.78 (s, 3H). Tr(METCR0990)=1.26 min (ES⁺) (M+H)⁺ 243.

Step 4, Method 82:5-Methoxy-N-[2-(1-Methyl-6-oxo-1,6-dihydropyridazin-3-yl)-1,3-benzoxazol-5-yl]pyridine-3-carboxamide

To a suspension of6-(5-amino-1,3-benzoxazol-2-yl)-2-methyl-2,3-dihydropyridazin-3-one(90%, 42 mg, 0.16 mmol) and 5-methoxypyridine-3-carboxylic acid (25 mg,0.16 mmol) in pyridine (2 mL) was added1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (39 mg, 0.2mmol) and the resulting suspension stirred for 1 hour. The reactionmixture was slowly diluted with water (5 mL) and the resultingsuspension stirred for 5 mins, before the solid was filtered off andair-dried. A hot ethanol trituration gave the title compound 27 mg (47%yield) as a red solid.

Example 1, Method 82:5-Methoxy-N-[2-(1-Methyl-6-oxo-1,6-dihydropyridazin-3-yl)-1,3-benzoxazol-5-yl]pyridine-3-carboxamide

δ_(H) NMR (500 MHz, DMSO) 10.61 (s, 1H), 8.76 (d, J=1.6 Hz, 1H), 8.50(d, J=2.8 Hz, 1H), 8.34 (d, J=1.8 Hz, 1H), 8.19 (d, J=9.7 Hz, 1H),7.90-7.83 (m, 2H), 7.79 (dd, J=8.8, 2.0 Hz, 1H), 7.15 (d, J=9.7 Hz, 1H),3.94 (s, 3H), 3.81 (s, 3H). Tr(METCR1600)=3.6 min (ES⁺) (M+H)⁺ 378.

The following examples were prepared using Method 82 described above:

TABLE 83 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

337.36 5-Methoxy-N-[2-(1- methyl-6-oxo-1,6- dihydropyridazin-3-yl)-1,3-benzoxazol- 5-yl]pyridine-2- carboxamide Tr(MET-uHPLC- AB-101) =2.69 min, (ES⁺) (M + H)⁺ 378 2

337.36 5-Methoxy-N-[2-(1- methyl-6-oxo-1,6- dihydropyridazin-3-yl)-1,3-benzoxazol- 5-yl]pyridine-3- carboxamide Tr(METCR1600) = 3.6min, (ES⁺) (M + H)⁺ 378 3

337.36 4-Methoxy-N-[2-(1- methyl-6-oxo-1,6- dihydropyridazin-3-yl)-1,3-benzoxazol- 5-yl]pyridine-2- carboxamide Tr(METCR1600) = 4.14min, (ES⁺) (M + H)⁺ 378 4

378.35 1-Methyl-N-[2-(1- methyl-6-oxo-1,6- dihydropyridazin-3-yl)-1,3-benzoxazol- 5-yl)-6-oxo-1,6- dihydropyridazine- 3-carboxamideTr(METCR1600) = 3.46 min, (ES⁺) (M + H)⁺ 379Method 83

Step 1, Method 83: Methyl 5-formylpyridine-3-carboxylate

Methyl 5-bromopyridine-3-carboxylate (3.82 g, 17.66 mmol), tert-butylisocyanide (2.4 mL, 21.2 mmol), triethylsilane (8.46 mL, 52.99 mmol),biphenyl-2-yl(dicyclohexyl)phosphane (0.28 g, 0.79 mmol) and disodiumcarbonate (1.87 g, 17.66 mmol) were suspended in N,N-dimethylformamide(40 mL) and the mixture degassed with nitrogen for 5 mins. Palladium(II)diacetate (0.12 g, 0.53 mmol) was added and the mixture heated at 65° C.overnight under nitrogen. The mixture was cooled to room temperature,diluted with water (200 mL) and ethyl acetate (40 mL), filtered,extracted with ethyl acetate (2×50 mL) then washed with water (5×25 mL),dried over sodium sulfate, filtered and concentrated. This material wasstirred in 1 M hydrochloric acid (50 mL) for 2 hours, cooled to 0° C.and quenched with 1 M sodium carbonate to pH 9. The mixture wasextracted with ethyl acetate (3×30 mL) dried over sodium sulfatefiltered and concentrated to give the title compound 0.95 g (33% yield)as an off-white powder. δ_(H) (500 MHz, DMSO) 10.20 (s, 1H), 9.31 (d,J=2.1 Hz, 1H), 9.29 (d, J=2.0 Hz, 1H), 8.68 (t, J=2.1 Hz, 1H), 3.94 (s,3H). Tr(METCR0990)=1.03 min, (ES⁺) (M+H)⁺ 166.

Step 2, Method 83: 5-Formylpyridine-3-carboxylic acid

Methyl 5-formylpyridine-3-carboxylate (0.95 g, 5.75 mmol) was dissolvedin tetrahydrofuran (20 mL) and water (20 mL) and lithium hydroxide (0.14g, 5.75 mmol) added and the mixture stirred at room temperatureovernight. Lithium hydroxide (0.14 g, 5.75 mmol) was added and themixture stirred for 2 hours. The organic solvent was evaporated and theaqueous layer washed with ethyl acetate (3×20 mL). The aqueous layer wasneutralised with 1 M hydrochloric acid to pH 3 and extracted with ethylacetate (3×20 mL) and 1:1 isopropanol:chloroform (3×10 mL). The combinedorganic fractions were dried over magnesium sulfate, filtered andconcentrated. The mixture was azeotroped with toluene (15 mL) twice togive the title compound 0.63 g (72.6% yield) as a white powder. δ_(H)(500 MHz, DMSO) 13.74 (s, 1H), 10.19 (s, 1H), 9.29 (d, J=2.1 Hz, 1H),9.26 (d, J=2.0 Hz, 1H), 8.66 (t, J=2.1 Hz, 1H).

Step 3, Method 83:5-Formyl-N-{2-hydroxy-5-[(5-methoxypyridin-2-yl)methoxy]phenyl}pyridine-3-carboxamide

5-Formylpyridine-3-carboxylic acid (95%, 200 mg, 1.26 mmol) and2-amino-4-[(5-methoxypyridin-2-yl)methoxy]phenol dihydrochloride (401.3mg, 1.26 mmol, prepared using Method 33) were stirred in pyridine (10mL) for 20 minutes. 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimidehydrochloride (313 mg, 1.63 mmol) was added and the mixture stirred atroom temperature under nitrogen overnight. Water (20 mL) was added andthe mixture extracted with 1:1 isopropanol:chloroform (3×25 mL) andwashed with water (2×10 mL). The combined organic layers were dried oversodium sulfate, filtered and concentrated to give a brown oil.Purification by FCC (silica, 0-10% methanol in dichloromethane) gave thetitle compound 0.07 g (13% yield) as a yellow solid. δ_(H) (500 MHz,DMSO) 10.20 (s, 1H), 9.90 (s, 1H), 9.33 (s, 1H), 9.23 (d, J=1.8 Hz, 1H),8.73 (s, 1H), 8.27 (d, J=2.9 Hz, 1H), 7.55-7.31 (m, 3H), 6.84 (d, J=8.8Hz, 1H), 6.75 (dd, J=8.8, 3.0 Hz, 1H), 5.02 (s, 2H), 3.83 (s, 3H), 3.17(s, 1H). Tr(METCR1673)=0.89 min, (ES⁺) (M+H)⁺380, 86%.

Step 4, Method 83:5-{5-[(5-Methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}pyridine-3-carbaldehyde

5-Formyl-N-{2-hydroxy-5-[(5-methoxypyridin-2-yl)methoxy]phenyl}pyridine-3-carboxamide(95%, 51 mg, 0.13 mmol) was suspended in acetic acid (2 mL) in amicrowave tube and the mixture heated to 180° C. for 90 mins. Thesolution was cooled to room temperature then concentrated to dryness.Purification by FCC (silica, 0-10% methanol in dichloromethane) gave thetitle compound 20 mg (37% yield) of as an off white powder. δ_(H) NMR(500 MHz, chloroform) 10.20 (s, 1H), 9.63 (d, J=2.1 Hz, 1H), 9.18 (d,J=2.0 Hz, 1H), 8.89 (t, J=2.1 Hz, 1H), 8.31 (d, J=2.8 Hz, 1H), 7.51 (d,J=8.9 Hz, 1H), 7.45 (d, J=8.6 Hz, 1H), 7.35 (d, J=2.5 Hz, 1H), 7.23 (dd,J=8.6, 2.9 Hz, 1H), 7.11 (dd, J=8.9, 2.5 Hz, 1H), 5.20 (s, 2H), 3.86 (s,3H). Tr(METCR1673)=1.04 min, (ES⁺) (M+H)⁺ 362, 86%.

Step 5, Method 83:[(5-{5-[(5-Methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}pyridin-3-yl)methyl](methyl)amine

5-{5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}pyridine-3-carbaldehyde(20 mg, 0.06 mmol) was dissolved in toluene (5 mL) and methanamine (33%wt in ethanol, 14 μl, 0.11 mmol) and magnesium sulfate (20 mg) added,and the mixture stirred for 10 minutes, filtered and concentrated.Toluene (5 mL), methanamine (33% wt in ethanol, 13.78 μl, 0.11 mmol) andmagnesium sulfate (20 mg) were added and the mixture stirred for 10minutes, filtered and concentrated. The residue was diluted withtoluene, methanamine (33% wt in ethanol, 13.78 μl, 0.11 mmol) andmagnesium sulfate were added and the mixture stirred overnight, filteredand evaporated. The mixture was dissolved in dichloromethane (50 mL), 2M methylamine in tetrahydrofuran (110 μl, 0.22 mmol) and magnesiumsulfate (246 mg) added and the mixture stirred overnight (the solventevaporated). The mixture was dissolved in dichloromethane (50 mL), 2 Mmethylamine in tetrahydrofuran (220 μl, 0.44 mmol) and magnesium sulfate(1 g) added and the mixture stirred overnight. The mixture was filteredand evaporated then put in a freezer under nitrogen for 1 week. Themixture was dissolved in dichloromethane (50 mL), 2 M methylamine intetrahydrofuran (220 μl, 0.44 mmol) and magnesium sulfate (1 g) addedand the mixture stirred overnight. The mixture was filtered andevaporated. The mixture was diluted with 1,2-dichloroethane (2 mL) andsodium triacetoxyborohydride (18 mg, 0.08 mmol) and acetic acid (1 drop)were added and the mixture stirred overnight. Water (5 mL) and saturatedsodium hydrogen carbonate solution (1 mL) were added and the mixtureextracted with dichloromethane (4×5 mL). The combined organic layerswere dried over sodium sulfate, filtered and concentrated. Purificationby FCC (silica, 0-50% (25% 7 N ammonia in methanol in dichloromethane)in dichloromethane) and preparative HPLC (acetonitrile/water+0.2%ammonium hydroxide) to give the title compound 10 mg (48% yield) as awhite powder.

Example 1, Method 83:[(5-{5-[(5-Methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}pyridin-3-yl)methyl](methyl)amine

δ_(H) NMR (500 MHz, Methanol) 9.27 (d, J=2.0 Hz, 1H), 8.72 (d, J=2.1 Hz,1H), 8.59 (t, J=2.1 Hz, 1H), 8.25 (d, J=2.8 Hz, 1H), 7.63 (d, J=8.9 Hz,1H), 7.57 (d, J=8.7 Hz, 1H), 7.45 (dd, J=8.6, 2.9 Hz, 1H), 7.38 (d,J=2.5 Hz, 1H), 7.16 (dd, J=8.9, 2.5 Hz, 1H), 5.20 (s, 2H), 3.91 (s, 2H),3.90 (s, 3H), 2.46 (s, 3H). Tr(MET-uHPLC-AB-101)=1.56 min, (ES⁺) (M+H)⁺377.

The following example was prepared using Method 83 described above:

TABLE 84 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

376.42 [(5-{5-[(5- Methoxypyridin-2- yl)methoxy]-1,3- benzoxazol-2-yl}pyridin-3- yl)methyl](methyl) amine Tr(MET-uHPLC- AB-101) = 1.56 min,(ES⁺) (M + H)⁺ 377Method 84

Step 1, Method 84:3-({2-Hydroxy-5-[(5-methoxypyridin-2-yl)methoxy]phenyl}carbamoyl)pyridin-1-ium-1-olate

2-Ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline (0.090 g, 0.36 mmol) wasadded to a suspension of nicotinic acid N-oxide (0.051 g, 0.37 mmol) indichloromethane (15 mL), and the mixture stirred at room temperatureunder nitrogen for 1 hour.2-Amino-4-[(5-methoxypyridin-2-yl)methoxy]phenol (0.100 g, 0.406 mmol,prepared using Method 33) was added, and the mixture stirred overnight.The precipitate was collected by filtration and dried under reducedpressure. Purification by FCC (silica, 0-10% methanol indichloromethane) gave the title compound 0.068 g (38% yield) as alight-brown solid: δ_(H) NMR (500 MHz, DMSO) 9.81 (br s, 1H), 9.23 (brs, 1H), 8.67 (s, 1H), 8.38 (d, J=6.0 Hz, 1H), 8.27 (d, J=2.5 Hz, 1H),7.79 (d, J=7.5 Hz, 1H), 7.55 (dd, J=7.5, 6.5 Hz, 1H), 7.46 (d, J=8.5 Hz,1H), 7.41 (dd, J=8.5, 3.0 Hz, 1H), 7.33 (d, J=3.0 Hz, 1H), 6.83 (d,J=8.5 Hz, 1H), 6.75 (dd, J=8.5, 3.0 Hz, 1H), 5.01 (s, 2H), 3.83 (s, 3H).

Step 2, Method 84:3-{5-[(5-Methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}pyridin-1-ium-1-olate

A mixture3-({2-hydroxy-5-[(5-methoxypyridin-2-yl)methoxy]phenyl}carbamoyl)pyridin-1-ium-1-olate(0.100 g, 0.272 mmol) and para-toluenesulfonic acid monohydrate (0.518g, 2.72 mmol) in glacial acetic acid (3 mL) was heated under microwaveirradiation at 120° C. for 2.5 hours. The reaction was cooled to roomtemperature and added dropwise to ice cold saturated sodium bicarbonatesolution. The pH of the resulting mixture was adjusted to 7 by addingsaturated sodium bicarbonate solution, and the product extracted intoethyl acetate (3×50 mL). The combined organics were dried over sodiumsulfate, filtered, and concentrated. Purification by FCC (silica, 0-10%methanol in dichloromethane) twice gave the title compound 0.055 g, (58%yield) as an off-white solid.

Example 1, Method 84:3-{5-[(5-Methoxypyridin-2-yl)methoxy]-1,3-benzoxazol-2-yl}pyridin-1-ium-1-olate

δ_(H) NMR (500 MHz, DMSO) 8.77-8.76 (m, 1H), 8.43-8.42 (m, 1H), 8.31 (d,J=3.0 Hz, 1H), 8.02-8.01 (m, 1H), 7.75 (d, J=9.0 Hz, 1H), 7.65-7.63 (m,1H), 7.53-7.50 (m, 2H), 7.43 (dd, J=9.0, 3.0 Hz, 1H), 7.17 (dd, J=9.0,2.5 Hz, 1H), 5.19 (s, 2H), 3.84 (s, 3H). Tr(METCR1416)=3.0 min, (ES⁺)(M+H)⁺ 350.

The following example was prepared using Method 84 described above:

TABLE 85 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

349.35 3-{5-[(5- Methoxypyridin-2- yl)methoxy]-1,3- benzoxazol-2-yl)pyridin-1-ium- 1-olate Tr(METCR1416) = 3.0 min, (ES⁺) (M + H)⁺ 350Method 85

Step 1, Method 85: 4-Hydroxy-3-(pyridine-3-amido)benzoic acid

3-Amino-4-hydroxybenzoic acid (0.5 g, 3.27 mmol) was dissolved inpyridine (5 mL) and 2-chloronicotinyl chloride hydrochloride (0.581 g,3.27 mmol) added and the mixture stirred overnight. Pyridine was removedin vacuo and the resulting oil dissolved in ethyl acetate and washedwith water twice. The organic layer was dried over magnesium sulfate,filtered and concentrated. Purification by FCC (silica, 30-70% ethylacetate in dichloromethane) and FCC (silica, 1-5% methanol indichloromethane) gave the tile compound 500 mg (59% yield) as an orangesolid. δ_(H) NMR (500 MHz, DMSO) 12.55 (s, 1H), 10.63 (s, 1H), 9.84 (s,1H), 9.13 (d, J=1.9 Hz, 1H), 8.83-8.73 (m, 1H), 8.33 (dt, J=7.9, 1.8 Hz,1H), 8.26 (d, J=2.0 Hz, 1H), 7.69 (dd, J=8.5, 2.1 Hz, 1H), 7.62-7.51 (m,1H), 7.00 (d, J=8.5 Hz, 1H). Tr(METCR1410)=1.15 min, (ES⁺) (M+H)⁺ 259,75%.

Step 2, Method 85: 2-(Pyridin-3-yl)-1,3-benzoxazole-5-carboxylic acid

4-Hydroxy-3-(pyridine-3-amido)benzoic acid (150 mg, 0.517 mmol) wasdissolved in acetic acid (3 mL) and heated in a microwave for 10 min at200° C. The solvent was removed and preparative HPLC(acetonitrile/water+0.2% ammonium hydroxide) gave the title compound 55mg (44% yield) as a white solid. δ_(H) NMR (500 MHz, DMSO) 9.38 (d,J=2.1 Hz, 1H), 8.82 (dd, J=4.8, 1.6 Hz, 1H), 8.57 (dt, J=8.0, 1.9 Hz,1H), 8.29 (s, 1H), 8.06 (dd, J=8.5, 1.5 Hz, 1H), 7.80 (d, J=8.5 Hz, 1H),7.67 (dd, J=8.0, 4.8 Hz, 1H). Tr(METCR1410)=0.96 min, (ES⁺) (M+H)⁺ 241.

Step 3, Method 85:N-(5-Methoxypyridin-3-yl)-2-(pyridin-3-yl)-1,3-benzoxazole-5-carboxamide

2-(Pyridin-3-yl)-1,3-benzoxazole-5-carboxylic acid (108 mg, 0.45 mmol)and 5-methoxypyridin-3-amine (56 mg, 0.45 mmol) were combined inpyridine (3 mL). 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimidehydrochloride (70 mg, 0.45 mmol) was added and the solution stirredovernight. The reaction was diluted with water (10 mL) and thenextracted with ethyl acetate (3×10 mL). The combined organics werewashed with water (2×10 mL), dried over magnesium sulfate, filtered andconcentrated. Purification by preparative HPLC (acetonitrile/water+0.1%formic acid) and preparative HPLC (acetonitrile/water+0.2% ammoniumhydroxide) gave the title compound 12 mg (8% yield) as a white solid.

Example 1, Method 85:N-(5-Methoxypyridin-3-yl)-2-(pyridin-3-yl)-1,3-benzoxazole-5-carboxamide

δ_(H) NMR (500 MHz, DMSO) 10.57 (s, 1H), 9.40 (d, J=1.4 Hz, 1H), 8.85(dd, J=4.8, 1.5 Hz, 1H), 8.61 (d, J=1.9 Hz, 1H), 8.59 (dt, J=8.0, 1.8Hz, 1H), 8.50 (d, J=1.2 Hz, 1H), 8.10 (dd, J=8.6, 1.7 Hz, 1H), 8.08 (d,J=2.6 Hz, 1H), 8.01 (d, J=8.6 Hz, 1H), 7.93 (t, J=2.3 Hz, 1H), 7.69 (dd,J=8.0, 4.8 Hz, 1H), 3.86 (s, 3H). Tr(METCR1600)=3.82 min, (ES⁺)(M+H)+347.

The following example was prepared using Method 85 described above:

TABLE 86 Mol. Ex. Structure Weight IUPAC Name LCMS data 1

346.35 N-(5- Methoxypyridin-3- yl)-2-(pyridin-3-yl)- 1,3-benzoxazole-5-carboxamide Tr(METCR1600) = 3.82 min, (ES⁺) (M + H)⁺ 347

Biology Examples

Q46 Radioligand Binding Assay

For radioligand binding assays (RBA) GST-Q46 protein was generated basedon a previous publication (Scherzinger et al. Cell, Vol. 90, 549-558,Aug. 8, 1997). For experiments 33 μM GST-Q46 was incubated with 150μg/mL thrombin in assay buffer (150 mM NaCl, 50 mM Tris pH 8.0) and 2 mMCaCl₂ for 16 hours at 37° C. Aggregated Q46 was pelleted bycentrifugation for 5 minutes at 13,000 rpm in a bench top centrifuge andre-dissolved in the same volume of assay buffer. Test compounds wereprepared by titration in DMSO at 11 concentrations from 33 μM to 1 nM.For the RBA, Q46 protein aggregates and test compounds werepre-incubated in assay buffer for 20 minutes at room temperature, in 140μL/well in a 96-well plate (pp, round bottom). Then, ligand was added in10 μL/well and incubated for 60 minutes at 37° C. Final assayconcentrations were 1 μM to 30 pM test compound, 5 μM Q46 protein(equivalent monomer concentration) and 10 nM ligand [³H3]MK-3328(Harrision et al., ACS Med. Chem. Lett., 2 (2011), pp 498-502). Sampleswere transferred onto GF/B filter plates and washed 2× with 200 μL PBSusing a Filtermate Harvester. After drying filter plates for 1 hour at37° C., the back of the plates were sealed with foil and 30 μL/wellscintillation fluid (Packard MicroScint 40) added, incubated for 15minutes in the dark and counted in a TopCount reader. For analysis,replicate data from independent assay plates were normalized towards 0%and 100% inhibition using control wells of vehicle (0% inhibition) and 3μM unlabelled MK-3328 (100% inhibition). IC₅₀ values were determinedwith a sigmoidal inhibition model with four variables (top, bottom,slope, IC₅₀) in a global fit using the normalized replicate data.

TABLE 87 RBA IC₅₀ activity summary: <100 nM +++, 100-500 nM ++, >50 nM +Structure IUPAC Name Activity

4-{[2-(4-chlorophenyl)-1,3- benzoxazol-5-yl]carbamoyl} phenyl acetate+++

N-(2-phenyl-1,3-benzoxazol-5- yl)benzamide +++

4-methoxy-N-[2-(3- methylphenyl)-1,3-benzoxazol- 5-yl]benzamide +++

2-methoxy-N-[2-(4- methoxyphenyl)-1,3- benzoxazol-5-yl]benzamide +++

4-methoxy-N-[2-(4- methoxyphenyl)-1,3- benzoxazol-5-yl]benzamide +++

3-methoxy-N-[2-(4- methoxyphenyl)-1,3- benzoxazol-5-yl]benzamide +++

4-methoxy-N-[2-(pyridin-3- yl)-1,3-benzoxazol-5-yl] benzamide +++

4-methoxy-N-[2-(pyridin-4- yl)-1,3-benzoxazol-5- yl]benzamide +++

N-[(4-methoxyphenyl)methyl]- 2-(pyridin-3-yl)-1,3- benzoxazol-5-amine+++

5-methoxy-N-[2-(3- methylphenyl)-1,3-benzoxazol-5-yl]pyridine-2-carboxamide +++

6-methoxy-N-[2-(3- methylphenyl)-1,3-benzoxazol-5-yl]pyridine-3-carboxamide +++

2-methoxy-N-[2-(3- methylphenyl)-1,3-benzoxazol-5-yl]pyrimidine-5-carboxamide +++

5-methoxy-N-[2-(3- methylphenyl)-1,3-benzoxazol-5-yl]pyrazine-2-carboxamide +++

4-methoxy-N-[2-(3- methylphenyl)[1,3]oxazolo[5,4-b]pyridin-6-yl]benzamide +++

5-(4-methoxyphenyl)-2- (pyridin-3-yl)-1,3-benzoxazole +++

N-(4-methoxyphenyl)-2- (pyridin-3-yl)-1,3-benzoxazol- 5-amine ++

2-(pyridin-3-yl)-N- {[1,2,4]triazolo[4,3-a]pyridin-3-yl}-1,3-benzoxazol-5-amine +++

2-(pyridin-3-yl)-N-(pyrimidin- 4-yl)-1,3-benzoxazol-5-amine +++

2-(pyridin-3-yl)-N-(pyrimidin- 2-yl)-1,3-benzoxazol-5-amine +++

5-(5-methoxypyrimidin-2-yl)- 2-(pyridin-3-yl)-1,3- benzoxazole +++

5-(6-methoxypyridazin-3-yl)-2- (pyridin-3-yl)-1,3-benzoxazole +++

5-(5-methoxypyridin-2-yl)-2- (pyridin-3-yl)-1,3-benzoxazole ++

5-(5-methoxypyrazin-2-yl)-2- (pyridin-3-yl)-1,3-benzoxazole +++

5-(2-methoxypyrimidin-5-yl)- 2-(pyridin-3-yl)-1,3- benzoxazole ++

4-[5-(pyrimidin-5-ylmethoxy)- 1-benzofuran-2-yl]pyridine-3- carbonitrile+++

4-{5-[(5-methoxypyridin-2- yl)methoxy]-1-benzofuran-2-yl}pyridine-3-carbonitrile +++

4-{5-[(5-methoxypyridin-2- yl)methoxy]-1-benzofuran-2- yl}pyridine +++

4-{5-[(1-methyl-1H-imidazol- 4-yl)methoxy]-1-benzofuran-2-yl}pyridine-3-carbonitrile +++

4-{5-[(1-methyl-1H-imidazol- 2-yl)methoxy]-1-benzofuran-2-yl}pyridine-3-carbonitrile ++

1-methyl-4-[5-(pyrimidin-5- ylmethoxy)-1-benzofuran-2-yl]-1H-pyrazole-3-carbonitrile +++

5-methoxy-2-[2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]-2,3-dihydro-1H-isoindol-1-one +++

3-{6-[(E)-2-(4-methoxyphenyl) ethenyl]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine +++

4-[5-(pyridin-3-yloxy)-1- benzofuran-2-yl]pyridine-3- carbonitrile +++

6-methoxy-2-[2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]-1,2,3,4-tetrahydroisoquinolin-1-one ++

5-[(4-methoxyphenyl) methoxy]-2-(pyridin-3-yl)-1,3- benzoxazole +++

5-[(3-methoxyphenyl) methoxy]-2-(pyridin-3-yl)-1,3- benzoxazole +++

5-[(5-methoxypyridin-2-yl) methoxy]-2-(pyridin-3-yl)-1,3- benzoxazole+++

2-(pyridin-3-yl)-5-(pyridin-3- ylmethoxy)-1,3-benzoxazole +++

5-[(1-methyl-1H-pyrazol-4- yl)methoxy]-2-(pyridin-3-yl)- 1,3-benzoxazole++

5-{5H,6H-imidazo[2,1-b][1,3] thiazol-3-ylmethoxy}-2-(pyridin-3-yl)-1,3-benzoxazole ++

dimethyl({3-[4-({[2-(pyridin-3- yl)-1,3-benzoxazol-5-yl]oxy}methyl)phenoxy]propyl}) amine +++

1-(pyridin-2-yl)-2-[2-(pyridin- 3-yl)-1,3-benzoxazol-5-yl] ethan-1-one++

1-(pyridin-2-yl)-2-[2-(pyridin- 3-yl)-1,3-benzoxazol-5-yl] ethan-1-ol ++

6-methoxy-2-[2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]-1,2-dihydroisoquinolin-1-one ++

2-(pyridin-3-yl)-N-[2,2,2- trifluoro-1-(4-methoxyphenyl)ethyl]-[1,3]oxazolo[5,4-b] pyridin-6-amine +

3-{6-[2-(4-methoxyphenyl) ethynyl]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine +++

3-{6-[(Z)-2-(4-methoxyphenyl) ethenyl]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine +++

5-methoxy-2-[2-(pyridin-3-yl)- [1,3]oxazolo[5,4-b]pyridin-6-yl]-2,3-dihydro-1H-isoindol-1- one +++

5-[(5-methoxypyrazin-2-yl) methoxy]-2-(pyridin-3-yl)-1,3- benzoxazole+++

3-methoxy-6-[2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]-5H,6H,7H-pyrrolo[3,4-b] pyridin-7-one +++

2-(pyridin-3-yl)-6-(pyridin-3- ylmethoxy)-1,3-benzoxazole +++

3-{6-[2-(pyridin-3-yl)ethynyl]- [1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine +++

5-{[(5-methoxypyridin-2-yl) oxy]methyl}-2-(pyridin-3-yl)-1,3-benzoxazole +++

4-[5-(pyridin-3-ylmethoxy)-1- benzofuran-2-yl]pyridine-3- carbonitrile+++

4-{5-[(1-methyl-1H-pyrazol-4- yl)methoxy]-1-benzofuran-2-yl}pyridine-3-carbonitrile +++

3-[5-(pyridin-3-ylmethoxy)-1- benzofuran-2-yl]pyridine-4- carbonitrile+++

3-{5-[(1-methyl-1H-pyrazol-4- yl)methoxy]-1-benzofuran-2-yl}pyridine-4-carbonitrile +++

3-{6-[1-(5-methoxypyridin-2- yl)ethoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine ++

4-{5-[(5-methoxypyrazin-2- yl)methoxy]-1-benzofuran-2-yl}pyridine-3-carbonitrile +++

6-({[2-(pyridin-3-yl)-1,3- benzoxazol-5-yl]oxy}methyl) pyridin-3-ol +++

5-{[5-(prop-2-en-1-yloxy) pyrazin-2-yl]methoxy}-2-(pyridin-3-yl)-1,3-benzoxazole +++

5-({[2-(pyridin-3-yl)-1,3- benzoxazol-5-yl]oxy}methyl)-1,2-dihydropyrazin-2-one ++

1-methyl-5-({[2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]oxy}methyl)-1,2-dihydropyrazin-2- one ++

5-[4-(5-methoxypyrimidin-2- yl)piperazin-1-yl]-2-(pyridin-3-yl)-1,3-benzoxazole +++

3-{6-[(5-methoxypyridin-2- yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine +++

5-(1-methyl-1H-pyrazol-4-yl)- 2-(pyridin-3-yl)-1,3- benzoxazole ++

3-{6-[(6-methoxypyridin-3- yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine +++

5-[(5-methoxypyridin-2-yl) methoxy]-2-(pyridin-4-yl)-1,3- benzoxazole+++

5-[(5-methoxypyridin-2-yl) methoxy]-2-(1-methyl-1H-pyrazol-4-yl)-1,3-benzoxazole +++

5-[(5-methoxypyridin-2-yl) methoxy]-2-(pyrazin-2-yl)-1,3- benzoxazole+++

[(3-{5-[(5-methoxypyridin-2- yl)methoxy]-1,3-benzoxazol-2-yl}phenyl)methyl] dimethylamine +++

5-[(5-methoxypyridin-2-yl) methoxy]-2-(1- methylpiperidin-4-yl)-1,3-benzoxazole ++

5-[(5-methoxypyridin-2-yl) methoxy]-2-(1,3-thiazol-5-yl)-1,3-benzoxazole +++

5-[2-(pyridin-2-yloxy)ethoxy]- 2-(pyridin-3-yl)-1,3- benzoxazole ++

4-[5-(1H-pyrazol-4- ylmethoxy)-1-benzofuran-2-yl]pyridine-3-carbonitrile +++

3-{[(2-{5H,6H-imidazo[2,1-b] [1,3]thiazol-3-yl}-1-benzofuran-5-yl)oxy]methyl} pyridine +++

7-{5-[(5-methoxypyridin-2- yl)methoxy]-1,3-benzoxazol-2-yl}-5,6,7,8-tetrahydro-1,7- naphthyridine +++

2-(1H-imidazol-1-yl)-5-[(5- methoxypyridin-2-yl)methoxy]-1,3-benzoxazole +++

2-{5H,6H,7H,8H-imidazo [1,2-a]pyrazin-7-yl}-5-[(5- methoxypyridin-2-yl)methoxy]-1,3-benzoxazole +++

2-(3-fluoroazetidin-1-yl)-5-[(5- methoxypyridin-2-yl)methoxy]-1,3-benzoxazole ++

2-{3H,4H,5H,6H,7H-imidazo [4,5-c]pyridin-5-yl}-5-[(5-methoxypyridin-2-yl) methoxy]-1,3-benzoxazole +++

5-[(5-methoxypyridin-2-yl) methoxy]-2- {2H,4H,5H,6H,7H-pyrazolo[4,3-c]pyridin-5-yl}-1,3- benzoxazole +++

2-{5H,6H,7H,8H-imidazo [1,5-a]pyrazin-7-yl}-5-[(5- methoxypyridin-2-yl)methoxy]-1,3-benzoxazole +++

5-[(5-methoxypyridin-2-yl) methoxy]-2-{5H,6H,7H-pyrrolo[3,4-b]pyridin-6-yl}- 1,3-benzoxazole +++

4-(5-{[1-(2-methoxyethyl)-1H- pyrazol-4-yl]methoxy}-1-benzofuran-2-yl)pyridine- 3-carbonitrile +++

N-(5-{5-[(5-methoxypyridin-2- yl)methoxy]-1,3-benzoxazol-2-yl}pyridin-2-yl)acetamide +++

5-{5-[(5-methoxypyridin-2- yl)methoxy]-1,3-benzoxazol-2-yl}pyridin-2-amine +++

2-[5-(2-methoxyethoxy) pyridin-3-yl]-5-[(5- methoxypyridin-2-yl)methoxy]-1,3-benzoxazole +++

methyl({[4-({[2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]oxy}methyl)phenyl]methyl})amine ++

4-(5-{[1-(2-hydroxyethyl)-1H- pyrazol-4-yl]methoxy}-1-benzofuran-2-yl)pyridine-3- carbonitrile +++

dimethyl({2-[4-({[2-(pyridin-3- yl)-1,3-benzoxazol-5-yl]oxy}methyl)phenoxy]ethyl})amine ++

5-{[5-(2-methoxyethoxy) pyridin-2-yl]methoxy}-2-(pyridin-3-yl)-1,3-benzoxazole +++

4-[5-({1-[2-(dimethylamino) ethyl]-1H-pyrazol-4-yl}methoxy)-1-benzofuran-2-yl] pyridine-3-carbonitrile +++

5-{5-[(5-methoxypyridin-2- yl)methoxy]-1,3-benzoxazol-2-yl}-N-methylpyridin-2-amine +++

3-{[(2-{2-bromo-5H,6H- imidazo[2,1-b][1,3]thiazol-3-yl}-1-benzofuran-5-yl)oxy] methyl}pyridine +++

5-[(5-methoxypyrazin-2-yl) methoxy]-2-(pyridin-3-yl)-1H-1,3-benzodiazole +++

5-[(5-methoxypyrazin-2-yl) methoxy]-1-methyl-2-(pyridin-3-yl)-1H-1,3-benzodiazole ++

6-[(5-methoxypyrazin-2-yl) methoxy]-1-methyl-2-(pyridin-3-yl)-1H-1,3-benzodiazole ++

5-[(5-methoxypyridin-2-yl) methoxy]-2-(piperazin-1-yl)- 1,3-benzoxazole+

N-methyl-6-({[2-(pyridin-3- yl)-1,3-benzoxazol-5-yl]oxy}methyl)pyridin-3-amine +++

3-[5-(pyridin-3-ylmethoxy)-1- benzofuran-2-yl]-5H,6H-imidazo[2,1-b][1,3]thiazole-2- carbonitrile +++

5-{5-[(5-methoxypyridin-2- yl)methoxy]-1,3-benzoxazol-2-yl}-N-methylpyridine-2- carboxamide +++

5-[(5-methoxypyridin-2- yl)methoxy]-2-(1-methyl-1H- imidazol-4-yl)-1,3-benzoxazole ++

5-methoxy-N-{[2-(pyridin-3- yl)-1,3-benzoxazol-5-yl]methyl}pyridin-2-amine ++

4-(5-{5H,6H-imidazo[2,1-b] [1,3]thiazol-3-ylmethoxy}-1-benzofuran-2-yl)pyridine-3- carbonitrile +++

5-({5-[2-(morpholin-4-yl) ethoxy]pyridin-2-yl}methoxy)-2-(pyridin-3-yl)-1,3- benzoxazole +++

2-bromo-6-{5-[(5- methoxypyridin-2-yl) methoxy]-1-benzofuran-2-yl]benzonitrile +++

2-(3-bromopyridin-4-yl)-6-[2- (morpholin-4-yl)ethoxy]-1,3- benzothiazole+++

tert-butyl 4-[2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]piperazine-1-carboxylate ++

3-{5-[(5-methoxypyridin-2- yl)methoxy]-1,3-benzoxazol-2-yl}pyridin-1-ium-1-olate +++

2-phenoxy-N-[2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]acetamide +++

N-[2-(pyridin-3-yl)-1,3- benzoxazol-5-yl]-1- benzofuran-2-carboxamide+++

N-[2-(pyridin-3-yl)-1,3- benzoxazol-5-yl]-6-(trifluoromethyl)pyridine-3- carboxamide +++

N-[2-(pyridin-3-yl)-1,3- benzoxazol-5-yl] quinoxaline-2-carboxamide +++

6-phenoxy-N-[2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]pyridine-3-carboxamide +++

N-[2-(pyridin-3-yl)-1,3- benzoxazol-5-yl]-2H-1,3-benzodioxole-5-carboxamide +++

3-(benzyloxy)-N-[2-(pyridin-3- yl)-1,3-benzoxazol-5-yl] benzamide +++

3-phenoxy-N-[2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]benzamide +++

N-[2-(pyridin-3-yl)-1,3- benzoxazol-5-yl] quinoline-2-carboxamide +++

N-[2-(pyridin-3-yl)-1,3- benzoxazol-5-yl]-2,3-dihydro-1-benzofuran-2-carboxamide +++

5-methyl-N-[2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]pyridine-3-carboxatmide +++

N-[2-(pyridin-3-yl)-1,3- benzoxazol-5-yl] quinoxaline-6-carboxamide +++

(2E)-3-(4-methoxyphenyl)-N- [2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]prop-2- enamide +++

5-methoxy-N-[2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]pyridine-2-carboxamide +++

3-cyano-N-[2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]benzamide +++

4-(methylsulfanyl)-N-[2- (pyridin-3-yl)-1,3-benzoxazol- 5-yl]benzamide+++

benzyl N-[2-(pyridin-3-yl)-1,3- benzoxazol-5-yl]carbamate +++

5-[2-(pyridin-3-yl)-1,3- benzoxazol-5-yl]pyrazin-2-ol ++

5-[(5-methoxypyridin-2-yl) methoxy]-2-(pyrimidin-5-yl)- 1,3-benzoxazole+++

2-(2,3-dihydro-1-benzofuran-2- yl)-5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazole +++

2-[(2R)-2,3-dihydro-1- benzofuran-2-yl]-5-[(5- methoxypyridin-2-yl)methoxy]-1,3-benzoxazole +++

2-[(2S)-2,3-dihydro-1- benzofuran-2-yl]-5- [(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazole +++

5-[5-(2-methoxyethoxy) pyrimidin-2-yl]-2-(pyridin-3- yl)-1,3-benzoxazole+++

5-[(5-methoxypyridin-2- yl)methoxy]-2-(5- methylpyridin-3-yl)-1,3-benzoxazole +++

5-[(5-methoxypyridin-2- yl)methoxy]-2- (2-methylpyridin-4-yl)-1,3-benzoxazole +++

5-[(5-methoxypyridin-2- yl)methoxy]-2-(3- phenoxyphenyl)-1,3-benzoxazole +++

6-{5-[(5-methoxypyridin-2- yl)methoxy]-1,3-benzoxazol-2-yl}-2-methyl-2,3- dihydropyridazin-3-one +++

5-[(5-methoxypyridin-2-yl) methoxy]-2-(pyridazin-3-yl)- 1,3-benzoxazole+++

5-[(5-methoxypyridin-2- yl)methoxy]-2-(pyridazin-4- yl)-1,3-benzoxazole+++

5-{5-[(5-methoxypyridin-2- yl)methoxy]-1,3-benzoxazol-2-yl}-1,2-dihydropyridin-2-one +++

5-{5-[(5-methoxypyridin-2- yl)methoxy]-1,3-benzoxazol-2-yl}-1-methyl-1,2- dihydropyridin-2-one +++

5-phenyl-N-[2-(pyridin-3-y])- 1,3-benzoxazol-5-yl]-1,3,4-oxadiazole-2-carboxamide +++

5-[(5-methoxypyridin-2-yl) methoxy]-2-(pyrimidin-4-yl)- 1,3-benzoxazole+++

5-[(5-bromopyridin-2-yl) methoxy]-2-(pyridin-3-yl)-1,3- benzoxazole +++

5-(pyridin-2-ylmethoxy)-2- (pyridin-3-yl)-1,3-benzoxazole ++

N-[2-(pyridin-3-yl)-1,3- benzoxazol-5-yl]-1- benzofuran-5-carboxamide+++

2-phenyl-N-[2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]pyrimidine-5-carboxamide +++

N-[2-(pyridin-3-yl)-1,3- benzoxazol-5-yl]-4-(pyrimidin- 2-yl)benzamide+++

1-methyl-N-[2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]-1H-pyrazole-4-carboxamide +++

4-[(6-methylpyrazin-2-yl)oxy]- N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]benzamide +++

4-(phenoxymethyl)-N-[2- (pyridin-3-yl)-1,3-benzoxazol- 5-yl]benzamide+++

2-phenoxy-N-[2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]pyridine-3-carboxamide +++

4-cyano-N-[2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]benzamide +++

6-methoxy-N-[2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]pyridine-2-carboxamide +++

2-methyl-N-[2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]pyridine-4-carboxamide +++

3-methoxy-N-[2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]pyridine-2-carboxamide ++

4-methoxy-N-[2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]pyridine-2-carboxamide +++

4-hydroxy-N-[2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]pyridine-2-carboxamide ++

3-methoxy-N-[2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]-1,2-oxazole-5-carboxamide +++

5-methoxy-N-[2-(pyridin-3-yl)- 1,3-benzoxazol-5-yl]pyridine-3-carboxamide +++

6-({[2-(1-methyl-1H-pyrazol- 4-yl)-1,3-benzoxazol-5-yl]oxy}methyl)pyridin-3-ol ++

5-[(5-methoxypyrazin-2- yl)methoxy]-2-(1-methyl-1H-pyrazol-4-yl)-1,3-benzoxazole +++

2-methoxy-5-({[2-(1-methyl- 1H-pyrazol-4-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl] oxy}methyl)pyrazine +++

3-{6-[(5-bromopyridin-2- yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridine +++

3-methoxy-6-({[2-(pyridin-3- yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)pyridazine +++

3-{5-[(5-methoxypyridin-2- yl)methoxy]-1,3-benzoxazol-2- yl]benzonitrile+++

4-{5-[(5-methoxypyridin-2- yl)methoxy]-1,3-benzoxazol-2- yl]benzonitrile+++

5-(1-methyl-1H-pyrazol-4-yl)- 2-({[2-(pyridin-3-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl] oxy}methyl)pyridine +++

3-methoxy-5-({[2-(pyridin-3- yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)pyridine +++

4-methoxy-2-({[2-(pyridin-3- yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)pyridine +++

2-({[2-(1-methyl-1H-pyrazol- 4-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl) pyrazine ++

[(3-{5-[(5-methoxypyridin-2- yl)methoxy]-1,3-benzoxazol-2-yl}phenyl)methyl](methyl) amine +++

(5-methoxypyridin-2-yl) methyl N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]carbamate +++

2-(5-methoxypyridin-2-yl)-5- [(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazole +++

2-(1-benzofuran-2-yl)-5-[(5- methoxypyridin-2-yl)methoxy]-1,3-benzoxazole +++

5-[(5-methoxypyridin-2-yl) methoxy]-2-[6-(trifluoromethyl)pyridin-3-yl]- 1,3-benzoxazole +++

2-(1-benzofuran-5-yl)-5-[(5- methoxypyridin-2-yl)methoxy]-1,3-benzoxazole +++

2-{5-[(5-methoxypyridin-2- yl)methoxy]-1,3-benzoxazol-2- yl}quinoline+++

2-[3-(benzyloxy)phenyl]-5-[(5- methoxypyridin-2-yl)methoxy]-1,3-benzoxazole +++

5-[(5-methoxypyridin-2-yl) methoxy]-2-[4-(pyrimidin-2-yl)phenyl]-1,3-benzoxazole +++

2-[(E)-2-(4-methoxyphenyl) ethenyl]-5-[(5-methoxypyridin-2-yl)methoxy]-1,3-benzoxazole +++

5-methoxy-2-({[2-(pyridin-3- yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)pyrimidine +++

6-({[2-(1-methyl-1H-pyrazol 4-yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl) pyridin-3-amine ++

5-{5-[(5-hydroxypyridin-2- yl)methoxy]-1,3-benzoxazol-2-yl}-N-methylpyridine-2- carboxamide +++

6-{6-[(5-methoxypyridin-2- yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}-2-methyl-2,3- dihydropyridazin-3-one +++

2-methyl-6-({[2-(pyridin-3-yl)- [1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)-2,3- dihydropyridazin-3-one ++

2-{6-[(5-methoxypyridin-2- yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl]pyrazine +++

5-{6-[(5-methoxypyridin-2- yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}-N- methylpyridine-2- carboxamide +++

5-{5-[(5-methoxypyridin-2- yl)methoxy]-1,3-benzoxazol-2-yl}-1-methyl-1,2- dihydropyrazin-2-one +++

6-(6-{[5-(2-fluoroethoxy) pyridin-2-yl]methoxy}-[1,3]oxazolo[5,4-b]pyridin-2-yl)-2- methyl-2,3-dihydropyridazin- 3-one +++

5-methoxy-2-({[2-(pyridin-3- yl)-[1,3]oxazolo[5,4-b]pyridin-6-yl]oxy}methyl)pyridin-1- ium-1-olate +++

3-{6-[(5-methoxy-1- oxidopyridin-1-ium-2- yl)methoxy]-[1,3]oxazolo[5,4-b]pyridin-2-yl}pyridin-1-ium- 1-olate ++

5-{5-[(5-methoxypyridin-2- yl)methoxy]-1,3-benzoxazol-2-yl}-2-(methylcarbamoyl) pyridin-1-ium-1-olate +++

(5-hydroxypyridin-2-yl)methyl N-[2-(pyridin-3-yl)-1,3-benzoxazol-5-yl]carbamate +++

5-methoxy-N-[2-(1-methyl-6- oxo-1,6-dihydropyridazin-3-yl)-1,3-benzoxazol-5-yl] pyridine-2-carboxamide +++

5-methoxy-N-[2-(1-methyl-6- oxo-1,6-dihydropyridazin-3-yl)-1,3-benzoxazol-5- yl]pyridine-3-carboxamide +++

4-methoxy-N-[2-(1-methyl-6- oxo-1,6-dihydropyridazin-3-yl)-1,3-benzoxazol-5-yl] pyridine-2-carboxamide +++

1-methyl-N-[2-(1-methyl-6- oxo-1,6-dihydropyridazin-3-yl)-1,3-benzoxazol-5-yl]-6- oxo-1,6-dihydropyridazine-3- carboxamide +++

[(5-{5-[(5-methoxypyridin-2- yl)methoxy]-1,3-benzoxazol-2-yl}pyridin-3-yl)methyl] (methyl)amine +++

6-{5-[(5-hydroxypyridin-2- yl)methoxy]-1,3-benzoxazol-2-yl}-2-methyl-2,3- dihydropyridazin-3-one +++

N-(5-methoxypyridin-3-yl)-2- (pyridin-3-yl)-1,3-benzoxazole-5-carboxamide +++In Vivo Imaging with [¹¹C]-Compound 3 of Method 14(5-[(5-[¹¹C-]-Methoxypyridin-2-yl)methoxy]-2-(pyridin-3-yl)-1,3-benzoxazole))in a Knock-in Model of Huntington's Disease

(5-[(5-[¹¹C-]-Methoxypyridin-2-yl)methoxy]-2-(pyridin-3-yl)-1,3-benzoxazole)was synthesized from 2-(pyridin-3-yl)-1,3-benzoxazol-5-ol (Method 14)via O-methylation, using [¹¹C]methyl triflate (obtained fromcyclotron-produced [¹¹C]methane) as an alkylating agent in the presenceof base according to the method of Chitneni, S. K. et al.: Synthesis andbiological evaluation of carbon-11-labeled acyclic andfuro[2,3-d]pyrimidine derivatives of bicyclic nucleoside analogues(BCNAs) for structure-brain uptake relationship study of BCNA tracers,Journal of Labelled Compounds and Radiopharmaceuticals 2008, 51,159-166. The incorporation rate was >80% and the radiochemical puritywas >99%. The labeled product was purified on semi-preparative HPLCcolumn (Ascentis RP-Amide C₁₈) using acetonitrile/aq. triethyl amine(0.1%) as eluent. The product was then concentrated using solid-phaseextraction procedure (on Waters tC₁₈ Vac 1 cc SPE cartridge) andformulated in sterile saline (0.9% NaCl) with >10% ethanol. Theradiochemical purity of the product was analyzed on an HPLC system usingAscentis RP-Amide C₁₈ analytical column and acetonitrile/aq. triethylamine (0.1%) as eluent, with sequential UV absorbance and radioactivitydetectors. The radiochemical purity of the formulated product wasdetermined to be >99%.

¹¹C-labeled Compound 3 of Method 14 was evaluated for its ability topenetrate the central nervous system of mice following systemicadministration, and its binding to the cerebellum, striatum,hippocampus, and cortex was quantitated. Three groups of animals werecompared: wild-type, and mice that were heterozygous or homozygous forthe zQ175 knock-in allele. (Menalled L. B. et al. Comprehensivebehavioral and molecular characterization of a new knock-in mouse modelof Huntington's disease: zQ175. PLoS One 2012, 7, e49838).

Forty-eight nine months old animals (16 WT, 16 heterozygous and 16homozygous zQ175) were obtained from The Jackson Laboratory, USA. Theanimals were housed at the animal department of Karolinska UniversityHospital in a temperature (±21° C.) and humidity (±40%) controlledenvironment on a 12 h light/dark cycle (lights on 7:00 AM) with accessto food and water ad libitum. Animals were allowed at least one week tohabituate to the animal department before the start of the imagingsessions. All experiments were conducted during the light phase of thecycle.

Animals were anesthetized with inhalation of isoflurane (4-5% isofluranein 100% oxygen). After induction of anesthesia, the isofluraneconcentration was lowered to 1.5-2% (50/50 air/oxygen) and the animalswere positioned in the scanner in a designated mouse bed. A cannula wasinserted in the tail vein through which the radioligand wasadministered. A 63-minute dynamic PET scan was initiated immediatelyupon intravenous injection of the radioligand. Upon completion of theimaging sessions, each animal was returned to its cage.

Image and Statistical Analysis

The acquired list mode data, was reconstructed into 25 timeframes (63min scan=4×10 s, 4×20 s, 4×60 s, 7×180 s, 6×360 s). The imagereconstruction was made with a fully 3-dimensional maximum-likelihoodexpectation maximization algorithm (MLEM) with 20 iterations, withoutscatter and attenuation correction. The reconstructed dynamic PET imageswere co-registered to an inbuilt mouse MRI template available in PMOD,which also incorporates volumes of interest (VOI's) sets (PMODTechnologies Ltd., Zurich, Switzerland). With the help of these VOIsets, decay corrected time activity curves (TAC) were generated. Theregional brain uptake values were expressed as percent standard uptakevalue (% SUV), which normalizes for injected radioactivity and bodyweight. In addition, the area under the curve (AUC) was calculated. Theselected regions of interest (ROI) were: cortex, hippocampus, striatumand cerebellum.

The average % SUV and AUC values for the ¹¹C-labeled Compound 3 ofMethod 14 in the four brain regions, for the three groups of mice, areshown in Table 88. Increased binding of the radioligand, relative towild type, was observed in all four brain regions in mice which werehomozygous for the zQ175 allele. FIG. 1 presents the AUC values for thethree groups of animals in the four regions of the brain.

TABLE 88 Average % SUV and AUC values of ¹¹C-labeled Compound 3 ofMethod 14 in the cortex, hippocampus, striatum and cerebellum of WT, hetzQ175 and hom zQ175 animals. Each value is expressed as Mean ± SD % SUVAUC WT Het Hom WT Het Hom (n = 7) (n = 7) (n = 6) (n = 7) (n = 7) (n =6) Cortex 69.1 ± 3.1 75.1 ± 4.3  93.9 ± 8.0 4965 ± 484 5685 ± 297 8233 ±883  Hippocampus 72.0 ± 3.6 80.3 ± 5.5 104.6 ± 7.9 4840 ± 402 5824 ± 3648983 ± 1078 Striatum 68.8 ± 2.7 79.7 ± 5.8 104.4 ± 9.1 4589 ± 311 5833 ±431 9006 ± 1205 Cerebellum 74.2 ± 3.0 78.4 ± 5.9  88.2 ± 5.0 4934 ± 3255570 ± 153 7118 ± 541 

Various modifications, additions, substitutions, and variations to theillustrative examples set forth herein will be apparent to those skilledin the art from the foregoing description. Such modifications are alsointended to fall within the scope of the appended claims.

What is claimed is:
 1. A compound of Formula (I), or a pharmaceuticallyacceptable salt thereof,

wherein X is O or S; Y is CR₄ or N; Z₁, Z₂, Z₃, and Z₄ are independentlychosen from CH and N, provided that at least two of Z₁, Z₂, Z₃, and Z₄are CH; R₁ is chosen from heteroaryl, heterocycloalkenyl, andheterocycloalkyl, each of which is optionally substituted with one ortwo groups independently chosen from cyano, halo, lower alkyl optionallysubstituted with amino, alkylamino, or di(alkyl)amino, lower alkoxyoptionally substituted with lower alkoxy, amino, alkylamino,di(alkyl)amino, haloalkyl, di(alkyl)aminocarbonyl, alkylaminocarbonyl,and aminocarbonyl, L₁ is —O— and L₂ is —(CR₇R₈)_(m)—; L₃ is absent; R₂is phenyl, pyridin-2-yl, pyridin-3-yl, pyrazin-2-yl, pyrimidin-5-yl,1H-imidazol-4-yl, 1H-imidazol-2-yl, or 1H-pyrazol-4-yl, each of which isoptionally substituted with one or two groups independently chosen fromhalo; haloalkyl; hydroxyl; lower alkoxy; lower alkoxy substituted withlower alkoxy, amino, (alkyl)amino, (dialkyl)amino, heterocycloalkyl,heteroaryl, or halo; lower alkyl; and lower alkyl substituted withhydroxyl, lower alkoxy, amino, (alkyl)amino, or (dialkyl)amino; R₄ ischosen from hydrogen, halo, cyano, and lower alkyl; R₅ is chosen fromlower alkyl, lower alkoxy, and halo; R₇ is chosen from hydrogen,hydroxyl, trifluoromethyl, and lower alkyl; R₈ is chosen from hydrogenand lower alkyl; n is 0 or 1; and m is 0, 1, or
 2. 2. The compound ofclaim 1, wherein R₁ is chosen from pyridin-2-yl, pyridin-3-yl,pyridin-3-yl-1-oxide, pyridin-4-yl, 1H-pyrazol-4-yl, pyrazin-2-yl,pyridazin-3-yl, pyridazin-4-yl, pyrimidin-4-yl, pyrimidin-5-yl,2,3-dihydropyridazin-3-one-6-yl, 1,2-dihydropyridin-2-one-5-yl,1,2-dihydropyrazin-2-one-5-yl, 1,3-thiazol-5-yl,5,6,7,8-tetrahydro-1,7-naphthyridine-7-yl, 1H-imidazol-1-yl,1-benzofuran-2-yl, 1-benzofuran-5-yl, 2,3-dihydro-1-benzofuran-2-yl,quinolone-2-yl, and 5H,6H,7H,8H-imidazo[1,2-a]pyrazin-7-yl, each ofwhich is optionally substituted with one or two groups independentlychosen from halo, lower alkyl, lower alkoxy, alkylamino, di(alkyl)amino,and amino.
 3. The compound of claim 1, wherein R₁ is

wherein W is chosen from N and N(O); p is chosen from 0, 1, and 2; foreach occurrence, R₉ is independently chosen from cyano, halo, loweralkyl, lower haloalkyl, lower alkyl substituted with —NR₁₀R₁₁, loweralkoxy, —C(O)NR₁₀R₁₁, and —NR₁₀R₁₁; R₁₀ is chosen from hydrogen andlower alkyl; and R₁₁ is chosen from hydrogen and lower alkyl.
 4. Thecompound of claim 1, wherein R₁ is

wherein W₁ and W₂ are chosen from CH and N, provided that at least oneof W₁ and W₂ is CH; p is chosen from 0, 1, and 2; and for eachoccurrence, R₉ is independently chosen from lower alkyl.
 5. The compoundof claim 1, wherein R₂ is pyridin-2-yl, pyridin-3-yl, pyrazin-2-yl,pyrimidin-5-yl, 1H-imidazol-4-yl, 1H-imidazol-2-yl, or 1H-pyrazol-4-yl,each of which is optionally substituted with one or two groupsindependently chosen from lower alkyl, hydroxyl, lower alkoxy, loweralkoxy substituted with amino, (alkyl)amino, (dialkyl)amino, or loweralkoxy, lower alkyl, and lower alkyl substituted with hydroxyl, loweralkoxy, amino, (alkyl)amino, or (dialkyl)amino.
 6. The compound of claim1, wherein X is O.
 7. The compound of claim 1, wherein X is S.
 8. Thecompound of claim 1, wherein Y is CR₄.
 9. The compound of claim 1,wherein Y is N.
 10. The compound of claim 1, wherein the compound islabeled with one or more positron-emitting radionuclides selected from:¹¹C, ¹³N, ¹⁵O, and ¹⁸F.
 11. A compound of Formula (I), or apharmaceutically acceptable salt thereof,

wherein X is NR₄, O, or S; Y is CR₄ or N; Z₁, Z₂, Z₃, and Z₄ areindependently chosen from CH and N, provided that at least two of Z₁,Z₂, Z₃, and Z₄ are CH; R₁ is heterocycloalkenyl or heterocycloalkyl,each of which is optionally substituted with one or two groupsindependently chosen from cyano, halo, lower alkyl optionallysubstituted with amino, alkylamino, or di(alkyl)amino, lower alkoxyoptionally substituted with lower alkoxy, optionally substituted amino,haloalkyl, di(alkyl)aminocarbonyl, alkylaminocarbonyl, andaminocarbonyl, or R₁ is phenyl optionally substituted with one or twogroups independently chosen from cyano, heteroaryl, halo, phenoxy,benzyloxy, lower alkyl optionally substituted with amino, (alkyl)amino,or di(alkyl)amino, lower alkoxy, optionally substituted amino,di(alkyl)aminocarbonyl, alkylaminocarbonyl, and aminocarbonyl; L₁ is—NR₃— and L₂ is —C(O)—, C—(R₇R₈)_(m)—, or —C(O)(R₇R₈)_(m)—; L₃ is—CH═CH— or L₃ is absent; R₂ is chosen from heterocycloalkyl, aryl andheteroaryl, each of which is optionally substituted with one or twogroups chosen from —OC(O)—R₆, —C(O)O—R₆, amino, halo, haloalkyl, phenyl,heteroaryl, cyano, (lower alkyl)thio, phenoxy, phenoxymethyl,heteroaryloxy, heteroaryloxy substituted with lower alkyl, hydroxyl,lower alkenyloxy, lower alkoxy, lower alkoxy substituted with loweralkoxy, amino, (alkyl)amino, (dialkyl)amino, heterocycloalkyl,heteroaryl, or halo, lower alkyl, and lower alkyl substituted withamino, (alkyl)amino, (dialkyl)amino, hydroxyl or lower alkoxy; R₃ ischosen from hydrogen and lower alkyl; R₄ is chosen from hydrogen, halo,cyano, and lower alkyl; R₅ is chosen from lower alkyl, lower alkoxy, andhalo; R₆ is lower alkyl; R₇ is chosen from hydrogen, hydroxyl,trifluoromethyl, and lower alkyl; R₈ is chosen from hydrogen and loweralkyl; n is 0 or 1; and m is 0, 1, or
 2. 12. The compound of claim 1,wherein R₁ is heterocycloalkenyl.
 13. The compound of claim 1, whereinR₁ is 2,3-dihydropyridazin-3-one-6-yl optionally substituted with one ortwo groups independently chosen from halo, lower alkyl, lower alkoxy,alkylamino, di(alkyl)amino, and amino.
 14. The compound of claim 1,wherein R₁ is 2,3-dihydropyridazin-3-one-6-yl substituted with one ortwo lower alkyl groups.
 15. The compound of claim 1, wherein R₂ ispyridin-2-yl optionally substituted with one or two groups independentlychosen from halo; haloalkyl; hydroxyl; lower alkoxy; lower alkoxysubstituted with lower alkoxy, amino, (alkyl)amino, (dialkyl)amino,heterocycloalkyl, heteroaryl, or halo; lower alkyl; and lower alkylsubstituted with hydroxyl, lower alkoxy, amino, (alkyl)amino, or(dialkyl)amino.
 16. The compound of claim 1, wherein R₂ is pyridin-2-ylsubstituted with lower alkoxy.
 17. The compound of claim 1, wherein Z₁,Z₂, Z₃, and Z₄ are independently CH.
 18. The compound of claim 11,wherein R₁ is heterocycloalkenyl.
 19. The compound of claim 11, whereinR₁ is 2,3-dihydropyridazin-3-one-6-yl optionally substituted with one ortwo groups independently chosen from halo, lower alkyl, lower alkoxy,alkylamino, di(alkyl)amino, and amino.
 20. The compound of claim 11,wherein R₁ is 2,3-dihydropyridazin-3-one-6-yl substituted with one ortwo lower alkyl groups.
 21. The compound of claim 11, wherein R₂ ispyridin-2-yl optionally substituted with one or two groups independentlychosen from halo; haloalkyl; hydroxyl; lower alkoxy; lower alkoxysubstituted with lower alkoxy, amino, (alkyl)amino, (dialkyl)amino,heterocycloalkyl, heteroaryl, or halo; lower alkyl; and lower alkylsubstituted with hydroxyl, lower alkoxy, amino, (alkyl)amino, or(dialkyl)amino.
 22. The compound of claim 11, wherein R₂ is pyridin-2-ylsubstituted with lower alkoxy.
 23. The compound of claim 11, wherein thecompound is labeled with one or more positron-emitting radionuclidesselected from: ¹¹C, ¹³N, ¹⁵O, and ¹⁸F.